Magnetic recording medium containing non-magnetic hematite particles as an undercoat layer

ABSTRACT

The present invention relates to acicular hematite particles containing aluminum of 0.05 to 50% by weight, calculated as Al, having an average major axial diameter of not more than 0.3 μm and a pH value of the particles of not less than 8, and containing soluble sodium salts of not more than 300 ppm soluble sodium, calculated as Na, and soluble sulfates of not more than 150 ppm soluble sulfate, calculated as SO 4 , which have an excellent dispersibility in a binder resin, and a magnetic recording medium which uses the hematite particles as non-magnetic particles for a non-magnetic undercoat layer, which has small light transmittance, smooth surface, high strength and high durability, and which is capable of suppressing the deterioration in the magnetic properties caused by a corrosion of the magnetic particles containing as a main ingredient in the magnetic recording layer.

This is a division of application Ser. No. 09/004,720, filed Jan. 8, 1998, now U.S. Pat. No. 6,120,898, the entire content of which is hereby incorporated by reference in this application.

BACKGROUND OF THE INVENTION

The present invention relates to hematite particles and a magnetic recording medium using hematite particles as non-magnetic particles for a non-magnetic undercoat layer. More particularly, the present invention relates to high-density acicular hematite particles which have an excellent dispersibility in a binder resin, and a magnetic recording medium which uses the hematite particles as non-magnetic particles for a non-magnetic undercoat layer, which has small light transmittance, smooth surface, high strength and high durability, and which is capable of suppressing the deterioration in the magnetic properties caused by a corrosion of the magnetic particles containing as a main ingredient (hereinafter refer to as “magnetic iron-based metal particles”) in the magnetic recording layer.

With a development of miniaturized and lightweight video or audio magnetic recording and reproducing apparatuses for long-time recording, magnetic recording media such as a magnetic tape and magnetic disk have been increasingly and strongly required to have a higher performance, namely, a higher recording density, higher output characteristic, in particular, an improved frequency characteristic and a lower noise level.

Various attempts have been made at both enhancing the properties of magnetic particles and reducing the thickness of a magnetic recording layer in order to improve these properties of a magnetic recording medium.

The enhancement of the properties of magnetic particles will first be described.

The properties which magnetic particles are required to have in order to satisfy the above-described demands on a magnetic recording medium, are a high coercive force and a large saturation magnetization.

As magnetic particles suitable for high-output and high-density recording, acicular magnetic iron-based metal particles which are obtained by heat-treating acicular goethite particles or acicular hematite particles in a reducing gas are widely known.

Although acicular magnetic iron-based metal particles have a high coercive force and a large saturation magnetization, since the acicular magnetic iron-based metal particles used for a magnetic recording medium are very fine particles having a particle size of not more than 1 μm, particularly, 0.01 to 0.3 μm, such particles easily corrode, and the magnetic properties thereof are deteriorated, especially, the saturation magnetization and the coercive force are reduced.

Therefore, in order to maintain the characteristics of a magnetic recording medium which uses magnetic iron-based metal particles as the magnetic particles, over a long period, it is strongly demanded to suppress the corrosion of acicular magnetic iron-based metal particles as much as possible.

A reduction in the thickness of a magnetic recording layer will now be described. Video tapes have recently been required more and more to have a higher picture quality, and the frequencies of carrier signals recorded in recent video tapes are higher than those recorded in conventional video tapes. In other words, the signals in the short-wave region have come to be used, and as a result, the magnetization depth from the surface of a magnetic tape has come to be remarkably small.

With respect to short wavelength signals, a reduction in the thickness of a magnetic recording layer is also strongly demanded in order to improve the high output characteristics, especially, the S/N ratio of a magnetic recording medium. This fact is described, for example, on page 312 of Development of Magnetic Materials and Technique for High Dispersion of Magnetic Powder, published by Sogo Gijutsu Center Co., Ltd. (1982), “ . . . the conditions for high-density recording in a coated-layer type tape are that the noise level is low with respect to signals having a short wavelength and that the high output characteristics are maintained. To satisfy these conditions, it is necessary that the tape has large coercive force Hc and residual magnetization Br, . . . and the coating film has a smaller thickness, . . . ”.

Development of a thinner film for a magnetic recording layer has caused some problems.

Firstly, it is necessary to make a magnetic recording layer smooth and to eliminate the non-uniformity of thickness. As well known, in order to obtain a smooth magnetic recording layer having a uniform thickness, the surface of the base film must also be smooth. This fact is described on pages 180 and 181 of Materials for Synthetic Technology-Causes of Friction and Abrasion of Magnetic Tape and Head Running System and Measures for Solving the Problem (hereinunder referred to as “Materials for Synthetic Technology” (1987), published by the Publishing Department of Technology Information Center, “ . . . the surface roughness of a hardened magnetic layer depends on the surface roughness of the substrate (back surface roughness) so largely as to be approximately proportional, . . . , since the magnetic layer is formed on the substrate, the more smooth the surface of the substrate is, the more uniform and larger head output is obtained and the more the S/N ratio is improved.”

Secondly, there has been caused a problem in the strength of a non-magnetic substrate such as a base film with a tendency of the reduction in the thickness of the non-magnetic substrate in response to the demand for a thinner magnetic layer. This fact is described, for example, on page 77 of the above-described Development of Magnetic Materials and Technique for High Dispersion of Magnetic Powder, “ . . . Higher recording density is a large problem assigned t the present magnetic tape. This is important in order to shorten the length of the tape so as to miniaturize the size of a cassette and to enable long-time recording. For this purpose, it is necessary to reduce the thickness of a substrate . . . With the tendency of reduction in the film thickness, the stiffness of the tape also reduces to such an extent as to make smooth travel in a recorder difficult. Therefore, improvement of the stiffness of a video tape both in the machine direction and in the transverse direction is now strongly demanded. “. . . ”

The end portion of a magnetic recording medium such as a magnetic tape, especially, a video tape is judged by detecting a portion of the magnetic recording medium at which the light transmittance is large by a video deck. If the light transmittance of the whole part of a magnetic recording layer is made large by the production of a thinner magnetic recording medium or the ultrafine magnetic particles dispersed in the magnetic recording layer, it is difficult to detect the portion having a large light transmittance by a video deck. For reducing the light transmittance of the whole part of a magnetic recording layer, carbon black or the like is added to the magnetic recording layer. It is, therefore, essential to add carbon black or the like to a magnetic recording layer in the present video tapes.

However, addition of a large amount of non-magnetic particles such as carbon black impairs not only the enhancement of the recording density but also the development of a thinner recording layer. In order to reduce the magnetization depth from the surface of the magnetic tape and to produce a thinner magnetic recording layer, it is strongly demanded to reduce, as much as possible, the quantity of non-magnetic particles such as carbon black which are added to a magnetic recording layer.

It is, therefore, strongly demanded that the light transmittance of a magnetic recording layer should be small even if the carbon black or the like which is added to the magnetic recording layer is reduced to a small amount. From this point of view, improvements in the substrate are now in strong demand.

There is no end to a demand for a higher performance in recent magnetic recording media. Since the above-described reduction in the thickness of a magnetic recording layer and a non-magnetic substrate lowers the durability of the surface of the magnetic recording layer and the magnetic recording medium, an improvement of the durability of the surface of the magnetic recording layer and the magnetic recording medium is in strong demand.

This fact is described in Japanese Patent Application Laid-Open (KOKAI) No. 5-298679, “ . . . With the recent development in magnetic recording, a high picture quality and a high sound quality have been required more and more in recording. The signal recording property is, therefore, improved. Especially, finer and higher-density ferromagnetic particles have come to be used. It is further required to make the surface of a magnetic tape smooth so as to reduce noise and raise the C/N . . . However, the coefficient of friction between the magnetic layer and an apparatus during the travel of the magnetic tape increases, so that there is a tendency of the magnetic layer of the magnetic recording medium being damaged or exfoliated even in a short time. Especially, in a video tape, since the magnetic recording medium travels at a high speed in contact with the video head, the ferromagnetic particles are apt to be dropped from the magnetic layer, thereby causing clogging on the magnetic head. Therefore, an improvement in the running stability of the magnetic layer of a magnetic recording medium is expected . . . ”.

Various efforts have been made to improve the base for a magnetic recording layer with a demand for a thinner magnetic recording layer and a thinner non-magnetic substrate. A magnetic recording medium having at least one undercoat layer (hereinunder referred to “non-magnetic undercoat layer”) comprising a binder resin and non-magnetic iron-based metal particles such as hematite particles which are dispersed therein, on a non-magnetic substrate such as a base film has been proposed and put to practical use (Japanese Patent Publication (KOKOKU) No. 6-93297 (1994), Japanese Patent Application Laid-Open (KOKAI) Nos. 62-159338 (1987), 63-187418 (1988), 4-167225 (1992), 4-325915 (1992), 5-73882 (1993), 5-182177 (1993), 5-347017 (1993), 6-60362 (1994), 9-22524 (1997), etc.)

For example, Japanese Patent Application Laid-Open (KOKAI) No. 5-182177 (1993) discloses a magnetic recording medium comprising: a non-magnetic substrate; a non-magnetic undercoat layer formed on the non-magnetic substrate and produced by dispersing inorganic particles in a binder resin; and a magnetic layer formed on the non-magnetic undercoat layer and produced by dispersing ferromagnetic particles in a binder resin while the non-magnetic undercoat layer is wet; wherein the magnetic layer has a thickness of not more than 1.0 μm in a dried state, the non-magnetic undercoat layer contains non-magnetic inorganic particles with surface layers coated with an inorganic oxide, the inorganic oxide coating the surfaces of the non-magnetic inorganic particles contained in the non-magnetic undercoat layer is at least one selected from the group consisting of Al₂O₃, SiO₂ and ZrO₂, and the amount of the inorganic oxide coating the non-magnetic inorganic particles is 1 to 21 wt % in the case of Al₂O₃, 0.04 to 20 wt % in the case of SiO₂, and 0.05 to 15 wt % in the case of ZrO₂, base on the total weigh of the magnetic inorganic particles.

Japanese Patent Application Laid-Open (KOKAI) No. 6-60362 (1994) discloses a non-magnetic undercoat layer for a magnetic recording medium formed on a non-magnetic substrate, comprising a coating film composition containing non-magnetic particles and a binder resin; wherein the non-magnetic particles are non-magnetic particles constituted by acicular α-Fe₂O₃ particles coated with an Al compound, and the non-magnetic particles constituted by acicular α-Fe₂O₃ particles coated with an Al compound have an average major axial diameter of 0.05 to 0.25 μm, an average minor axial diameter of 0.010 to 0.035 μm, a particle size distribution of not more than 1.40 in geometrical standard deviation, and an aspect ratio (major axial diameter/minor axial diameter) of 2 to 20.

However, the above-described non-magnetic particles are not particles which contain aluminum substantially uniformly from the central portions to the surfaces of the particles but particles which have an aluminum compound on the surfaces thereof.

A magnetic recording medium which has small light transmittance, high strength, smooth surface and higher durability, and which is capable of suppressing a corrosion of the acicular magnetic iron-based metal particles dispersed in the magnetic recording layer, with reduction of the thickness of not only the magnetic recording layer but also the non-magnetic substrate is now in the strongest demand, but no such magnetic recording medium which sufficiently satisfies these conditions have ever been obtained.

The above-described magnetic recording media composed of a non-magnetic substrate and a non-magnetic undercoat layer produced by dispersing non-magnetic particles in a binder resin and formed on a non-magnetic substrate, have a small light transmittance, a smooth surface and a high strength, but the durability thereof is inconveniently poor.

This fact is described in Japanese Patent Application Laid-Open (KOKAI) No. 5-182177 (1993), “ . . . Although the problem of surface roughness is solved by providing a magnetic layer as an upper layer after forming a thick non-magnetic undercoat layer on the surface of a substrate, the problem of the abrasion of a head and the problem of durability are not solved and still remain. This is considered to be caused because a thermoset resin is ordinarily used as a binder of the undercoat layer so that the magnetic layer is brought into contact with a head or other members without any cushioning owing to the hardened undercoat layer, and a magnetic recording medium having such an undercoat layer has a considerably poor flexibility.

In addition, it has been pointed out that in the known magnetic recording media, the magnetic iron-based metal particles which are dispersed in the magnetic recording layer cause a corrosion after production, thereby greatly deteriorating the magnetic properties.

Also, the demand for the enhancement of the surface smoothness in a magnetic recording medium has become increasingly stronger, and the thinner magnetic recording layer, the smoother surface is strongly demanded.

As a result of studies undertaken by the present inventors so as to solve the above-described problems, it has been found that by using specific acicular hematite particles as the non-magnetic particles for a non-magnetic undercoat layer of a magnetic recording medium, the obtained magnetic recording medium has small light transmittance, smooth surface, high strength and high durability, and it is capable of suppressing the deterioration in the magnetic properties by preventing a corrosion of the magnetic particles in a magnetic recording layer. The present invention has been achieved on the basis of this finding.

SUMMARY OF THE INVENTION

Accordingly, it is an object of the present invention to provide acicular hematite particles suitable as non-magnetic particles for a non-magnetic undercoat layer of a magnetic recording medium which has small light transmittance, smooth surface, high strength and high durability, and which is capable of suppressing the deterioration in the magnetic properties caused by a corrosion of the magnetic particles, especially, magnetic iron-based metal particles, contained in the magnetic recording layer.

It is another object of the present invention to provide a magnetic recording medium which has small light transmittance, high strength, smoother surface, and higher durability, and which is capable of suppressing the deterioration in the magnetic properties caused by a corrosion of the magnetic particles, especially, magnetic iron-based metal particles, contained in a magnetic recording layer.

To accomplish the aims, in an aspect of the present invention, there are provided acicular hematite particles containing aluminum of 0.05 to 50% by weight, calculated as Al, having an average major axial diameter of not more than 0.3 μm and a pH value of the particles of not less than 8, and containing soluble sodium salts of not more than 300 ppm soluble sodium, calculated as Na, and soluble sulfates of not more than 150 ppm soluble sulfate, calculated as SO₄.

In a second aspect of the present invention, there is provided acicular hematite particles containing aluminum of 0.05 to 50% by weight, calculated as Al; having a coating comprising at least one selected from the group consisting of a hydroxide of aluminum, an oxide of aluminum, a hydroxide of silicon and an oxide of silicon, which is coated on the surfaces of said acicular hematite particles; having an average major axial diameter of not more than 0.3 μm and a pH value of the particles of not less than 8; and containing soluble sodium salts of not more than 300 ppm soluble sodium, calculated as Na, and soluble sulfates of not more than 150 ppm soluble sulfate, calculated as SO₄.

In a third aspect of the present invention, there is provided a magnetic recording medium comprising: a non-magnetic substrate; a non-magnetic undercoat layer comprising a coating film composition comprising non-magnetic acicular hematite particles set forth in first or second aspect and a binder resin, which is formed on said non-magnetic substrate; and a magnetic recording layer comprising a coating film composition comprising magnetic particles containing iron as a main ingredient and a binder resin, which is formed on said non-magnetic undercoat layer.

In a fourth aspect of the present invention, there is provided magnetic recording medium comprising: a non-magnetic substrate; a non-magnetic undercoat layer comprising a coating film composition comprising non-magnetic acicular hematite particles and a binder resin, which is formed on said non-magnetic substrate; and a magnetic recording layer comprising a coating film composition comprising magnetic particles containing iron as a main ingredient and a binder resin, which is formed on said non-magnetic undercoat layer, wherein said non-magnetic acicular hematite particles contain 0.05 to 50 wt % of aluminum, calculated as Al, within the particle, have an average major axial diameter of not more than 0.3 μm, a pH value of said particles of not less than 8, and contain soluble sodium salts of not more than 300 ppm soluble sodium, calculated as Na and soluble sulfates of not more than 150 ppm soluble sulfate, calculated as SO₄; and said magnetic particles containing iron as a main ingredient comprising iron and aluminum of 0.05 to 10% by weight, calculated as Al.

In a fifth aspect of the present invention, there is provided a magnetic recording medium comprising: a non-magnetic substrate; a non-magnetic undercoat layer comprising a coating film composition comprising non-magnetic acicular hematite particles set forth in first or second aspect and a binder resin, which is formed on said non-magnetic substrate; and a magnetic recording layer comprising a coating film composition comprising binder resin and magnetic particles containing iron as a main ingredient comprising 50 to 99% by weight of iron, 0.05 to 10% by weight of aluminum, and at least one selected from the group consisting of Co, Ni, P, Si, B, Nd, La and Y, which is formed on said non-magnetic undercoat layer.

In a sixth aspect of the present invention, there is provided a magnetic recording medium comprising: a non-magnetic substrate; a non-magnetic undercoat layer comprising a coating film composition comprising non-magnetic acicular hematite particles set forth in first or second aspect and a binder resin, which is formed on said non-magnetic substrate; and a magnetic recording layer comprising a coating film composition comprising a binder resin and magnetic particles containing iron as a main ingredient comprising 50 to 99% by weight of iron, 0.05 to 10% by weight of aluminum, and at least one rare earth metal selected from the group consisting of Nd, La and Y, which is formed on said non-magnetic undercoat layer.

In a seventh aspect of the present invention, there is provided a magnetic recording medium comprising: a non-magnetic substrate; a non-magnetic undercoat layer comprising a coating film composition comprising non-magnetic acicular hematite particles set forth in second aspect and a binder resin, which is formed on said non-magnetic substrate; and a magnetic recording layer comprising a coating film composition comprising a binder resin and magnetic particles containing iron as a main ingredient comprising iron as a main ingredient comprising iron and aluminum of 0.05 to 10% by weight, calculated as Al, which is formed on said non-magnetic undercoat layer.

DETAILED DESCRIPTION OF THE INVENTION

The constitution of the present invention will be explained in more detail.

Acicular hematite particles (1) as non-magnetic particles according to the present invention will first be described.

The acicular hematite particles according to the present invention contain 0.05 to 50 wt % of aluminum (calculated as Al) approximately uniformly within the particles.

It is possible to obtain acicular hematite particles containing aluminum approximately uniformly within the particles by in case where acicular goethite particles are produced by passing an oxygen-containing gas such as air into a suspension containing the iron-containing precipitate such as iron hydroxide, iron carbonate or the like obtained by reacting a ferrous salt with an alkali hydroxide and/or an alkali carbonate, passing of the oxygen-containing gas into the suspension in the presence of the aluminum compound, thereby producing acicular goethite particles containing aluminum substantially uniformly from the central portions to the surfaces of the particles, and dehydrating the acicular goethite particles.

When the aluminum content within the acicular hematite particles is less than 0.05 wt % (calculated as Al), a magnetic recording medium having a non-magnetic undercoat layer containing such acicular hematite particles does not have a sufficient durability. If the aluminum content exceeds 50 wt %, although a magnetic recording medium having the non-magnetic undercoat layer containing such acicular hematite particles has a sufficient durability, the durability-improving effect becomes saturated, so that it is meaningless to add aluminum more than necessary. From the point of view of durability of a magnetic recording medium, the aluminum content therein is preferably 0.5 to 50 wt %, more preferably 1.0 to 50 wt %.

The acicular hematite particles in the present invention have an aspect ratio (average major axial diameter/average minor axial diameter) (hereinunder referred to merely as “aspect ratio”) of not less than 2:1, preferably not less than 3:1. The upper limit of the aspect ratio is ordinarily 20:1, preferably 10:1 with the consideration of the dispersibility in the vehicle. The shape of the acicular particles here may have not only acicular but also spindle-shaped, rice ball-shaped or the like.

If the aspect ratio is less than 2:1, it is difficult to obtain a desired film strength of the magnetic recording medium.

The average major axial diameter of the acicular hematite particles of the present invention is not more than 0.3 μm, preferably 0.005 to 0.3 μm. If the average major axial diameter exceeds 0.3 μm, the particle size is so large as to impair the surface smoothness. On the other hand, if the average-major axial diameter is less than 0.005 μm, dispersion in the vehicle may be unfavorably apt to be difficult. With the consideration of the dispersibility in the vehicle and the surface smoothness of the coated film, the more preferable average major axial diameter is 0.02 to 0.2 μm.

The average minor axial diameter of the acicular hematite particles of the present invention is preferably 0.0025 to 0.15 μm. If the average minor axial diameter is less than 0.0025 μm, dispersion in the vehicle may be unfavorably difficult. On the other hand if the average minor axial diameter exceeds 0.15 μm, the particle size may be apt to become so large as to impair the surface smoothness. With the consideration of the dispersibility in the vehicle and the surface smoothness of the coated film, the more preferable average minor axial diameter is 0.01 to 0.10 μm.

The pH value of the acicular hematite particles of the present invention is not less than 8. If it is less than 8, the magnetic iron-based metal particles contained in the magnetic recording layer formed on the non-magnetic undercoat layer are gradually corroded, thereby causing a deterioration in the magnetic properties. With the consideration of a corrosion preventive effect on the magnetic iron-based metal particles, the pH value of the particles is preferably not less than 8.5, more preferably not less than 9.0. The upper limit is ordinarily 12, preferably 11, more preferably 10.5.

The content of soluble sodium salts in the acicular hematite particles of the present invention is not more than 300 ppm soluble sodium (calculated as Na). If it exceeds 300 ppm, the magnetic iron-based metal particles contained in the magnetic recording layer formed on the non-magnetic undercoat layer are gradually corroded, thereby causing a deterioration in the magnetic properties. In addition, the dispersion property of the acicular hematite particles in the vehicle is easily impaired, and the preservation of the magnetic recording medium is deteriorated and efflorescence is sometimes caused in a highly humid environment. With the consideration of a corrosion preventive effect on the magnetic iron-based metal particles, the content of soluble sodium salt is preferably not more than 250 ppm, more preferably not more than 200 ppm, even more preferably not more than 150 ppm. From the point of view of industry such as productivity, the lower limit thereof is preferably about 0.01 ppm.

The content of soluble sulfate in the acicular hematite particles of the present invention is not more than 150 ppm soluble sulfate (calculated as SO₄). If it exceeds 150 ppm, the magnetic iron-based metal particles contained in the magnetic recording layer formed on the non-magnetic undercoat layer are gradually corroded, thereby causing a deterioration in the magnetic properties. In addition, the dispersion property of the acicular hematite particles in the vehicle is easily impaired, and the preservation of the magnetic recording medium is deteriorated and efflorescence is sometimes caused in a highly humid environment. With the consideration of a corrosion preventive effect on the magnetic iron-based metal particles, the content of soluble sulfate is preferably not more than 70 ppm, more preferably not more than 50 ppm. From the point of view of industry such as productivity, the lower limit thereof is preferably about 0.01 ppm.

The BET specific surface area of the acicular hematite particle of the present invention is ordinarily not less than 35 m²/g. If it is less than 35 m²/g, the acicular hematite particles may be coarse or sintering may be sometimes caused between particles, which are apt to exert a deleterious influence on the surface smoothness of the coated film. The BET surface area is more preferably not less than 40 m²/g, even more preferably not less than 45 m²/g, and the upper limit thereof is ordinarily 300 m²/g. The upper limit is preferably 100 m²/g, more preferably 80 m²/g with the consideration of the dispersibility in the vehicle.

The major axial diameter distribution of the acicular hematite particles of the present invention is preferably not more than 1.50 in geometrical standard deviation. If it exceeds 1.50, the coarse particles existent sometimes exert a deleterious influence on the surface smoothness of the coated film. The major axial diameter distribution is more preferably not more than 1.40, even more preferably not more than 1.35 in geometrical standard deviation with the consideration of the surface smoothness of the coated film. From the point of view of industrial productivity, the major axial diameter distribution of the acicular hematite particles obtained is ordinarily 1.01 in geometrical standard deviation.

In the acicular hematite particles of the present invention, the degree of densification is high. The degree of densification represented by the ratio of the specific surface area S_(BET) measured by a BET method and the surface area S_(TEM) calculated from the major axial diameter and the minor axial diameter which were measured from the particles in an electron micrograph is ordinarily 0.5 to 2.5.

With the consideration of the surface smoothness of the coated film and the dispersibility in the vehicle, the S_(BET)/S_(TEM) value is preferably 0.7 to 2.0, more preferably 0.8 to 1.6.

The resin adsorptivity of the acicular hematite particles of the present invention is ordinarily not less than 70%, preferably not less than 75%, more preferably not less than 80%.

The amount of sintering preventive existent on the surfaces of the acicular hematite particles of the present invention varies depending upon various conditions such as the kind of sintering preventive, the pH value thereof in an aqueous alkali solution and the heating temperature, it is ordinarily not more than 10 wt %, preferably 0.05 to 10 wt % based on the total weight of the particles.

The surfaces of the acicular hematite particles of the present invention may be coated with at least one selected from the group consisting of a hydroxide of aluminum, an oxide of aluminum, a hydroxide of silicon and an oxide of silicon. When the acicular hematite particles coated with the above-described coating material are dispersed in a vehicle, they have an affinity with the binder resin and it is easy to obtain a desired dispersibility.

The amount of aluminum hydroxide, aluminum oxide, silicon hydroxide or silicon oxide used as the coating material is ordinarily not less than 50 wt %, preferably 0.01 to 50 wt % (calculated as Al or SiO₂) . If it is less than 0.01 wt %, the dispersibility improving effect may be insufficient. If the amount exceeds 50.00 wt %, the coating effect becomes saturated, so that it is meaningless to add a coating material more than necessary. From the point of view of dispersibility in the vehicle, the preferable amount of coating material is preferably 0.05 to 20 wt % (calculated as Al or SiO₂).

Various properties of the acicular hematite particles coated with a coating material of the present invention, such as aspect ratio, average major axial diameter, average minor axial diameter, pH value, the content of soluble sodium salt, content of soluble sulfate, BET specific surface area, major axial diameter distribution, degree of densification, resin adsorptivity and amount of sintering preventive are approximately equivalent in values to those of the acicular hematite particles of the present invention the surfaces of which are not coated with a coating material.

The process for producing the acicular hematite particles according to the present invention will now be described.

In order to produce the acicular hematite particles of the present invention, acicular goethite particles containing aluminum within the particles are produced. Acicular goethite particles are produced by an ordinary method such as (A) a method of oxidizing a suspension having a pH value of not less than 11 and containing colloidal ferrous hydroxide particles which is obtained by adding not less than an equivalent of an alkali hydroxide solution to an aqueous ferrous salt solution, by passing an oxygen-containing gas thereinto at a temperature of not higher than 80° C.; (B) a method of producing spindle-shaped goethite particles by oxidizing a suspension containing FeCO₃ which is obtained by reacting an aqueous ferrous salt solution with an aqueous alkali carbonate solution, by passing an oxygen-containing gas thereinto after aging the suspension, if necessary; (C) a method of growing acicular seed goethite particles by oxidizing a ferrous hydroxide solution containing colloidal ferrous hydroxide particles which is obtained by adding less than an equivalent of an alkali hydroxide solution or an alkali carbonate solution to an aqueous ferrous salt solution, by passing an oxygen-containing gas thereinto, thereby producing acicular seed goethite particles, adding not less than an equivalent of an alkali hydroxide solution to the Fe²⁺ in the aqueous ferrous salt solution, to the aqueous ferrous salt solution containing the acicular goethite seed particles, and passing an oxygen-containing gas into the aqueous ferrous salt solution; and (D) a method of growing acicular seed goethite particles by oxidizing a ferrous hydroxide solution containing colloidal ferrous hydroxide particles which is obtained by adding less than an equivalent of an alkali hydroxide solution or an alkali carbonate solution to an aqueous ferrous salt solution, by passing an oxygen-containing gas thereinto, thereby producing acicular seed goethite particles, and growing the obtained acicular seed goethite particles in an acidic or neutral region.

The acicular goethite particles containing aluminum within the particles are obtained by passing the oxygen-containing gas such as air into the suspension of the iron-containing precipitate or aqueous solution of the ferrous salt, alkali hydroxide or alkali carbonate, which contain an aluminum compound.

It is essential that an aluminum compound is existent in the above-mentioned suspension or aqueous solution before passing the oxygen-containing gas such as air thereinto in the process for producing the goethite particles. To state this concretely, an aluminum compound may be added to any of the aqueous ferrous salt solution, the aqueous alkali hydroxide solution, the aqueous alkali carbonate solution and the suspension containing an iron-containing precipitate. It is the more preferable to add an aluminum compound to the aqueous ferrous salt solution.

Elements other than Fe and Al such as Ni, Zn, P and Si, which are generally added in order to enhance various properties of the particles such as the major axial diameter, the minor axial diameter and the aspect ratio, may be added during the reaction system for producing the goethite particles.

The acicular goethite particles obtained have an average major axial diameter of ordinarily 0.005 to 0.4 μm, an average minor axial diameter of ordinarily 0.0025 to 0.20 μm and a BET specific of about ordinarily 50 to 250 m²/g, and contain ordinarily soluble sodium salts of 300 to 1500 ppm soluble sodium (calculated as Na) and ordinarily soluble sulfates of 100 to 3000 ppm soluble sulfate (calculated as SO₄).

High-density acicular hematite particles containing aluminum within the particles are obtained by heating the acicular goethite particles containing aluminum within the particles at a temperature as high as not less than 550° C. In order to obtain high-density acicular hematite particles which retain the shapes of the acicular goethite particles, it is preferable to obtain low-density acicular hematite particles containing aluminum within the particles by heat-treating the acicular goethite particles at a low temperature, for example, 250 to 500° C. and then to heat the low-density acicular hematite particles at a high temperature, for example, not less than 550° C.

It is preferred to coat the particles with a sintering preventive before the heat-treatment at a low temperature or a high temperature in order to obtain high-density acicular hematite particles which retain the shapes of the acicular goethite particles. The acicular goethite particles coated with a sintering preventive contain soluble sodium salts of ordinarily 500 to 2000 ppm soluble sodium calculated as Na) and soluble sulfates of ordinarily 300 to 3000 ppm soluble sulfate (calculated as SO₄), and have the BET specific surface area of ordinarily about 50 to 250 m²/g. The coating treatment using a sintering preventive is composed of the steps of: adding a sintering preventive to an aqueous suspension containing the acicular goethite particles, mixing and stirring the suspension, filtering out the particles, washing the particles with water, and drying the particles.

As the sintering preventive, sintering preventives generally used are usable. For example, phosphorus compounds such as sodium hexametaphosphate, polyphospholic acid and orthophosphoric acid, silicon compounds such as #3 water glass, sodium orthosilicate, sodium metasilicate and colloidal silica, boron compounds such as boric acid, aluminum compounds including aluminum salts such as aluminum acetate, aluminum sulfate, aluminum chloride and aluminum borate, alkali aluminate such as sodium aluminate, and alumina sol, and titanium compounds such as titanyl sulfate may be exemplified.

The acicular hematite particles containing aluminum within the particles are obtained by heat-treating the acicular goethite particles containing aluminum within the particles at a temperature of 250 to 850° C.

The low-density acicular hematite particles obtained by heat-treating the acicular goethite particles coated with a sintering preventive at a temperature of 250 to 500° C. have an average major axial diameter of ordinarily 0.005 to 0.30 μm, an average minor axial diameter of ordinarily 0.0025 to 0.15 μm, a BET specific surface area of ordinarily about 70 to 350 m²/g and contain soluble sodium salts of ordinarily 500 to 2000 ppm soluble sodium (calculated as Na) and soluble sulfates of ordinarily 300 to 4000 ppm soluble sulfate (calculated as SO₄). If the temperature for heat-treating the goethite particles is less than 250° C., the dehydration reaction takes a long time. On the other hand, if the temperature exceeds 500° C., the dehydration reaction is abruptly brought out, so that it is difficult to retain the shapes because the sintering between particles is caused. The low-density acicular hematite particles obtained by heat-treating the goethite particles at a low temperature are low-density particles having a large number of dehydration pores through which H₂O is removed from the goethite particles and the BET specific surface area thereof is about 1.2 to 2 times larger than that of the acicular hematite particles as the starting material.

The low-density hematite particles are then heat-treated at a temperature of not less than 550° C. to obtain a high-density acicular hematite particles. The upper limit of the heating temperature is preferably 850° C. The high-density hematite particles contain soluble sodium salts of ordinarily 500 to 4000 ppm soluble sodium (calculated as Na) and soluble sulfates of ordinarily 300 to 5000 ppm soluble sulfate (calculated as SO₄), and the BET specific surface area thereof is ordinarily about 35 to 150 m²/g.

If the heat-treating temperature is less than 550° C., since the densification is insufficient, a large number of dehydration pores exist within and on the surface of the hematite particles, so that the dispersion in the vehicle is insufficient. Further, when the non-magnetic undercoat layer is formed from these particles, it is difficult to obtain a coated film having a smooth surface. On the other hand, if the temperature exceeds 850° C., although the densification of the hematite particles is sufficient, since sintering is caused on and between particles, the particle size increases, so that it is difficult to obtain a coated film having a smooth surface.

The acicular hematite particles are pulverized by a dry-process, and formed into a slurry. The slurry is then pulverized by a wet-process so as to deagglomerate coarse particles. In the wet-pulverization, ball mill, sand grinder, colloid mill or the like is used until coarse particles having a particle size of at least 44 μm are substantially removed. That is, the wet-pulverization is carried out until the amount of the coarse particles having a particle size of not less than 44 μm becomes to not more than 10% by weight, preferably not more than 5% by weight, more preferably 0% by weight based on the total weight of the particles. If the amount of the coarse particles having a particle size of not less than 44 μm is more than 10% by weight, the effect of treating the particles in an aqueous alkali solution at the next step is not attained.

The acicular hematite particles with coarse particles removed therefrom are heat-treated in a slurry at a temperature of not less than 80° C. after the pH value of the slurry is adjusted to not less than 13 by adding an aqueous alkali solution such as sodium hydroxide.

The concentration of the alkali suspension containing the acicular hematite particles and having a pH value of not less than 13 is preferably 50 to 250 g/liter.

If the pH value of the alkali suspension containing the acicular hematite particles is less than 13, it is impossible to effectively remove the solid crosslinking caused by the sintering preventive which exists on the surfaces of the hematite particles, so that it is impossible to wash out the soluble sodium slat, soluble sulfate, etc. existing within and on the surfaces of the particles. The upper limit of the pH value is ordinarily about 14. If the effect of removing the solid crosslinking caused by the sintering preventive which exists on the surfaces of the hematite particles, the effect of washing out the soluble sodium slat, soluble sulfate, etc., and the effect of removing the alkali which adheres to the surfaces of hematite particles in the process of the heat-treatment of the aqueous alkali solution are taken into consideration, the preferable pH value is in the range of 13.1 to 13.8.

The heat-treating temperature in the aqueous alkali solution is preferably not less than 80° C., more preferably not less than 90° C. If the temperature is less than 80° C., it is difficult to effectively remove the solid crosslinking caused by the sintering preventive which exists on the surfaces of the hematite particles. The upper limit of the heating temperature is preferably 103° C., more preferably 100° C. If the heating temperature exceeds 103° C., although it is possible to effectively remove the solid crosslinking, since an autoclave or the like is necessary or solution boils under a normal pressure, it is not advantageous from the point of view of industry.

The acicular hematite particles heat-treated in the aqueous alkali solution are thereafter filtered out and washed with water by an ordinary method so as to remove the soluble sodium salt and soluble sulfate which are washed out of the interiors and the surfaces of the particles and the alkali adhered to the surfaces of the hematite particles in the process of heat-treatment with the aqueous alkali solution, and then dried.

As the method of washing the particles with water, a method generally industrially used such as a decantation method, a dilution method using a filter thickener and a method of passing water into a filter press is adopted.

If the soluble sodium salt and soluble sulfate which are contained within the hematite particles are washed out with water, even if soluble sodium salt and soluble sulfate adhere to the surfaces when the surfaces of the hematite particles are coated with a coating material in a subsequent step, for example, the later-described coating step, they can be easily removed by water washing.

The acicular hematite particles of the present invention are filtered out and washed with water by an ordinary method after they are heat-treated in the aqueous alkali solution. Thereafter, the acicular hematite particles may be coated with at least one selected from the group consisting of a hydroxide of aluminum, an oxide of aluminum, a hydroxide of silicon and an oxide of silicon, if necessary.

In order to coat the hematite particles, an aluminum compound and/or a silicon compound is added to and mixed with an aqueous suspension under stirring which is obtained by dispersing the cake, slurry or dried particles of the acicular hematite particles into an aqueous solution. The pH value of the mixed solution is adjusted, if necessary. The acicular particles thus coated with at least one selected from the group consisting of a hydroxide of aluminum, an oxide of aluminum, a hydroxide of silicon and an oxide of silicon are then filtered out, washed with water, dried and pulverized. They may be further deaerated and compacted, if necessary.

As the aluminum compound for the coating, the same aluminum compounds as those described above as the sintering preventive are usable.

The amount of aluminum compound added is 0.01 to 50.00 wt % (calculated as Al) based on the weight of the acicular hematite particles. If the amount is less than 0.01 wt %, the improvement of the dispersibility in the vehicle may be insufficient. On the other hand, if the amount exceeds 50.00 wt %, the coating effect becomes saturated, so that it is meaningless to add an aluminum compound more than necessary.

As the silicon compound, the same silicon compounds as those described above as the sintering preventive are usable.

The amount of silicon compound added is 0.01 to 50.00 wt % (calculated as SiO₂) based on the weight of the acicular hematite particles. If the amount is less than 0.01 wt %, the improvement of the dispersibility in the vehicle may be insufficient. On the other hand, if the amount exceeds 50.00 wt %, the coating effect becomes saturated, so that it is meaningless to add an silicon compound more than necessary.

When both an aluminum compound and a silicon compound are used, the amount thereof used is preferably 0.01 to 50.00 wt % (calculated as Al and SiO₂) based on the weight of the acicular hematite particles.

A magnetic recording medium according to the present invention will now be explained.

The magnetic medium of according to the present invention comprises a non-magnetic substrate, a non-magnetic undercoat layer and a magnetic recording layer.

The non-magnetic undercoat layer in the present invention is produced by forming a coating film on the non-magnetic substrate and drying the coating film. The coating film is formed by applying a non-magnetic coating film composition which contains acicular hematite particles, a binder resin and a solvent, to the surface of the non-magnetic substrate.

As the non-magnetic substrate, the following materials which are at present generally used for the production of a magnetic recording medium are usable as a raw material: a synthetic resin such as polyethylene terephthalate, polyethylene, polypropylene, polycarbonate, polyethylene naphthalate, polyamide, polyamideimide and polyimide; foil and plate of a metal such as aluminum and stainless steel; and various kinds of paper. The thickness of the non-magnetic substrate varies depending upon the material, but it is ordinarily about 1.0 to 300 μm, preferably 2.0 to 200 μm. In the case of a magnetic disc, polyethylene terephthalate is ordinarily used as the non-magnetic substrate. The thickness thereof is ordinarily 50 to 300 μm, preferably 60 to 200 μm. In the case of a magnetic tape, when polyethylene terephthalate is used as the non-magnetic substrate, the thickness thereof is ordinarily 3 to 100 μm, preferably 4 to 20 μm. When polyethylene naphthalate is used, the thickness thereof is ordinarily 3 to 50 μm, preferably 4 to 20 μm. When polyamide is used, the thickness thereof is ordinarily 2 to 10 μm, preferably 3 to 7 μm.

The thickness of the undercoat layer obtained by coating the non-magnetic substrate with a coating film composition and drying the coating film, is ordinarily 0.2 to 10.0 μm, preferably 0.5 to 5.0 μm. If the thickness is less than 0.2 μm, not only it is impossible to ameliorate the surface roughness of the base film but also the strength is insufficient.

As the binder resin in the present invention, the following resins which are at present generally used for the production of a magnetic recording medium are usable: vinyl chloride-vinyl acetate copolymer, urethane resin, vinyl chloride-vinyl acetate-maleic acid copolymer, urethane elastomer, butadiene-acrylonitrile copolymer, polyvinyl butyral, cellulose derivative such as nitrocellulose, polyester resin, synthetic rubber resin such as polybutadiene, epoxy resin, polyamide resin, polyisocyanate resin, electron radiation curing acryl urethane resin and mixtures thereof. Each of these resin binders may contain a functional group such as —OH, —COOH, —SO₃M, —OPO₂M₂ and —NH₂, wherein M represents H, Na or K. With the consideration of the dispersibility of the particles, a binder resin containing a functional group —COOH or —SO₃M is preferable.

The mixing ratio of the acicular hematite particles with the binder resin is ordinarily 5 to 2000 parts by weight, preferably 100 to 1000 parts by weight based on 100 parts by weight of the binder resin.

It is possible to add a lubricant, a polishing agent, an antistatic agent, etc. which are generally used for the production of a magnetic recording medium to the non-magnetic undercoat layer.

The gloss of the coated film of the non-magnetic undercoat layer containing acicular hematite particles according to the present invention is ordinarily 180 to 280%, preferably 190 to 280%, more preferably 200 to 280% and the surface roughness Ra thereof is ordinarily 1.0 to 12.0 nm, preferably 1.0 to 10.0 nm, more preferably 2.0 to 9.0 nm, even more preferably 2.0 to 8.0 nm. The Young's modulus (relative value to a commercially available video tape: AV T-120 produced by Victor Company of Japan, Limited) thereof is ordinarily 125 to 150, preferably 127 to 150, more preferably 130 to 150.

The magnetic recording medium according to the present invention is produced by forming the non-magnetic undercoat layer formed on the non-magnetic substrate, forming a coating film on the non-magnetic undercoat layer by applying a coating film composition containing magnetic iron-based metal particles, a binder resin and a solvent, and drying the coating film to obtain a magnetic recording layer.

The magnetic particles containing iron as a main ingredient, that is, magnetic iron-based metal particles used in the present invention comprises iron and at least one selected from the group consisting of Co, Al, Ni, P, Si, Zn, Ti, Cu, B, Nd, La and Y. Further, the following magnetic iron-based metal particles may be exemplified.

1) Magnetic iron-based metal particles comprises iron; and Co of ordinarily 0.05 to 40 wt %, preferably 1.0 to 35 wt %, more preferably 3 to 30 wt % (calculated as Co) based on the weight of the magnetic iron-based metal particles.

2) Magnetic iron-based metal particles comprises iron; and Al of ordinarily 0.05 to 10 wt %, preferably 0.1 to 7 wt % (calculated as Al) based on the weight of the magnetic iron-based metal particles.

3) Magnetic iron-based metal particles comprises iron; Co of ordinarily 0.05 to 40 wt %, preferably 1.0 to 35 wt %, more preferably 3 to 30 wt % (calculated as Co) based on the weight of the magnetic iron-based metal particles; and Al of ordinarily 0.05 to 10 wt %, preferably 0.1 to 7 wt % (calculated as Al) based on the weight of the magnetic iron-based metal particles.

4) Magnetic iron-based metal particles comprises iron; Co of ordinarily 0.05 to 40 wt %, preferably 1.0 to 35 wt %, more preferably 3 to 30 wt % (calculated as Co) based on the weight of the magnetic iron-based metal particles; and at least one selected from the group consisting of Nd, La and Y of ordinarily 0.05 to 10 wt %, preferably 0.1 to 7 wt % (calculated as the corresponding element) based on the weight of the magnetic iron-based metal particles.

5) Magnetic iron-based metal particles comprises iron; Al of ordinarily 0.05 to 10 wt %, preferably 0.1 to 7 wt % (calculated as Al) based on the weight of the magnetic iron-based metal particles; and at least one selected from the group consisting of Nd, La and Y of ordinarily 0.05 to 10 wt %, preferably 0.1 to 7 wt % (calculated as the corresponding element) based on the weight of the magnetic iron-based metal particles.

6) Magnetic iron-based metal particles comprises iron; Co of ordinarily 0.05 to 40 wt %, preferably 1.0 to 35 wt %, more preferably 3 to 30 wt % (calculated as Co) based on the weight of the magnetic iron-based metal particles; Al of ordinarily 0.05 to 10 wt %, preferably 0.1 to 7 wt % (calculated as Al) based on the weight of the magnetic iron-based metal particles; and at least one selected from the group consisting of Nd, La and Y of ordinarily 0.05 to 10 wt %, preferably 0.1 to 7 wt % (calculated as the corresponding element) based on the weight of the magnetic iron-based metal particles.

7) Magnetic iron-based metal particles comprises iron; Co of ordinarily 0.05 to 40 wt %, preferably 1.0 to 35 wt %, more preferably 3 to 30 wt % (calculated as Co) based on the weight of the magnetic iron-based metal particles; and at least one selected from the group consisting of Ni, P, Si, Zn, Ti, Cu and B of ordinarily 0.05 to 10 wt %, preferably 0.1 to 7 wt % (calculated as the corresponding element) based on the weight of the magnetic iron-based metal particles.

8) Magnetic iron-based metal particles comprises iron; Al of ordinarily 0.05 to 10 wt %, preferably 0.1 to 7 wt % (calculated as Al) based on the weight of the magnetic iron-based metal particles; and at least one selected from the group consisting of Ni, P, Si, Zn, Ti, Cu and B of ordinarily 0.05 to 10 wt %, preferably 0.1 to 7 wt % (calculated as the corresponding element) based on the weight of the magnetic iron-based metal particles.

9) Magnetic iron-based metal particles comprises iron; Co of ordinarily 0.05 to 40 wt %, preferably 1.0 to 35 wt %, more preferably 3 to 30 wt % (calculated as Co) based on the weight of the magnetic iron-based metal particles; Al of ordinarily 0.05 to 10 wt %, preferably 0.1 to 7 wt % (calculated as Al) based on the weight of the magnetic iron-based metal particles; and at least one selected from the group consisting of Ni, P, Si, Zn, Ti, Cu and B of ordinarily 0.05 to 10 wt %, preferably 0.1 to 7 wt % (calculated as the corresponding element) based on the weight of the magnetic iron-based metal particles.

10) Magnetic iron-based metal particles comprises iron; Co of ordinarily 0.05 to 40 wt %, preferably 1.0 to 35 wt %, more preferably 3 to 30 wt % (calculated as Co) based on the weight of the magnetic iron-based metal particles; at least one selected from the group consisting of Nd, La and Y of ordinarily 0.05 to 10 wt %, preferably 0.1 to 7 wt % (calculated as the corresponding element) based on the weight of the magnetic iron-based metal particles; and at least one selected from the group consisting of Ni, P, Si, Zn, Ti, Cu and B of ordinarily 0.05 to 10 wt %, preferably 0.1 to 7 wt % (calculated as the corresponding element) based on the weight of the magnetic iron-based metal particles.

11) Magnetic iron-based metal particles comprises iron; Al of ordinarily 0.05 to 10 wt %, preferably 0.1 to 7 wt % (calculated as Al) based on the weight of the magnetic iron-based metal particles; at least one selected from the group consisting of Nd, La and Y of ordinarily 0.05 to 10 wt %, preferably 0.1 to 7 wt % (calculated as the corresponding element) based on the weight of the magnetic iron-based metal particles; and at least one selected from the group consisting of Ni, P, Si, Zn, Ti, Cu and B of ordinarily 0.05 to 10 wt %, preferably 0.1 to 7 wt % (calculated as the corresponding element) based on the weight of the magnetic iron-based metal particles.

12) Magnetic iron-based metal particles comprises iron; Co of ordinarily 0.05 to 40 wt %, preferably 1.0 to 35 wt %, more preferably 3 to 30 wt % (calculated as Co) based on the weight of the magnetic iron-based metal particles; Al of ordinarily 0.05 to 10 wt %, preferably 0.1 to 7 wt % (calculated as Al) based on the weight of the magnetic iron-based metal particles; at least one selected from the group consisting of Nd, La and Y of ordinarily 0.05 to 10 wt %, preferably 0.1 to 7 wt % (calculated as the corresponding element) based on the weight of the magnetic iron-based metal particles; and at least one selected from the group consisting of Ni, P, Si, Zn, Ti, Cu and B of ordinarily 0.05 to 10 wt %, preferably 0.1 to 7 wt % (calculated as the corresponding element) based on the weight of the magnetic iron-based metal particles.

The iron content in the particles is the balance, and is preferably 50 to 99 wt %, more preferably 60 to 95 wt % (calculated as Fe) based on the weight of the magnetic iron-based metal particles.

The magnetic iron-based metal particles comprising (i) iron and Al; (ii) iron, Co and Al, (iii) iron, Al and at least one rare-earth metal such as Nd, La and Y, or (iv) iron, Co, Al and at least one rare-earth metal such as Nd, La and Y is preferable from the point of the durability of the magnetic recording medium. Further, the magnetic iron-based metal particles comprising iron, Al and at least one rare-earth metal such as Nd, La and Y is more preferable.

With respect to the existing position of aluminum of ordinarily 0.05 to 10 wt % (calculated as Al) based on the weight of the magnetic iron-based metal particles, it may be contained only in the core and inside portions, or in the surface portion of the magnetic iron-based metal particles. Alternatively, aluminum may be approximately uniformly contained in the magnetic iron-based metal particles from the core portion to the surface. An aluminum-coating layer may be formed on the surfaces of the particles. In addition, any of these positions may be combined. In the consideration of the effect of improving the surface property of the magnetic recording layer or the durability of the magnetic recording medium, magnetic iron-based metal particles uniformly containing aluminum from the core portion to the surface and coated with an aluminum-coating layer are more preferable.

When the content of aluminum is less than 0.05 wt % (calculated as Al), the adsorption of the resin to the magnetic iron-based metal particles in the vehicle may not be said sufficient, so that it may be difficult to produce a magnetic recording layer or a magnetic recording medium having a high durability. When the content of aluminum exceeds 10 wt %, the effect of improving the durability of the magnetic recording layer or the magnetic recording medium is observed, but the effect is saturated and it is meaningless to add aluminum more than necessary. Further more, the magnetic characteristics of the magnetic iron-based metal particles may be sometimes deteriorated due to an increase in the aluminum as a non-magnetic component. The existing amount of aluminum of the magnetic iron-based metal particles is preferably 0.1 to 7% by weight.

It is more preferable to produce a magnetic recording medium of the present invention using the magnetic iron-based metal particles containing Al and a rare-earth metal such as Nd, La and Y therein, because the magnetic recording layer or magnetic recording medium produced is apt to have a more excellent durability. Especially, magnetic iron-based metal particles containing Al and Nd therein are the even more preferable.

The acicular magnetic iron-based alloy particles containing aluminum within the particles are produced, as is well known, by adding an aluminum compound at an appropriate stage during the above-described process for producing acicular goethite particles to produce acicular goethite particles containing aluminum at desired positions of the particles, and heat-treating, at a temperature of 300 to 500° C. the goethite particles or the acicular hematite particles containing aluminum at desired positions within the particles which are obtained by dehydrating the goethite particles.

The acicular magnetic iron-based metal particles coated with aluminum are produced by heat-treating, at a temperature of 300 to 500° C., the acicular goethite particles coated with an oxide or-hydroxide of aluminum, or the acicular hematite particles coated with the oxide or hydroxide of aluminum which are obtained by dehydrating the goethite particles.

The acicular magnetic iron-based metal particles used in the present invention have an average major axial diameter of ordinarily 0.01 to 0.50 μm, preferably 0.01 to 0.30 μm, more preferably 0.01 to 0.20 μm, an average minor axial diameter of ordinarily 0.0007 to 0.17 μm, preferably 0.003 to 0.10 μm, and an aspect ratio of ordinarily not less than 3:1, preferably and not less than 5:1. The upper limit of the aspect ratio is ordinarily 15:1, preferably 10:1 with the consideration of the dispersibility in the vehicle. The shape of the acicular magnetic iron-based metal particles may have not only acicular but also a spindle-shaped, rice ball-shaped or the like.

As to the magnetic properties of the acicular magnetic iron-based metal particles used in the present invention, the coercive force is preferably 1200 to 3200 Oe, more preferably 1500 to 2500 Oe, and the saturation magnetization is ordinarily preferably 100 to 170 emu/g, more preferably 130 to 170 emu/g with t he consideration of the properties such as high-density recording.

The resin adsorptivity of the acicular magnetic iron-based metal particles used in the present invention is ordinarily not less than 65%, preferably not less than 68%, more preferably not less than 70%, most preferably not less than 80%.

As the binder resin for the magnetic recording layer, the same binder resin as that used for the production of the non-magnetic undercoat layer is usable.

The thickness of the magnetic recording layer obtained by applying the film-coating composition to the non-magnetic undercoat layer and dried, is ordinarily in the range of 0.01 to 5.0 μm. If the thickness is less than 0.01 μm, uniform coating may be difficult, so that unfavorable phenomenon such as unevenness on the coating surface is observed. On the other hand, when the thickness exceeds 5.0 μm, it may be difficult to obtain desired signal recording property due to an influence of diamagnetism. The preferable thickness is in the range of 0.05 to 1.0 μm.

The mixing ratio of the acicular magnetic iron-based metal particles with the binder resin in the magnetic recording layer is ordinarily 200 to 2000 parts by weight, preferably 300 to 1500 parts by weight based on 100 parts by weight of the binder resin.

It is possible to add a lubricant, a polishing agent, an antistatic agent, etc. which are generally used for the production of a magnetic recording medium to the magnetic recording layer.

The magnetic recording medium according to the present invention has a coercive force of ordinarily 900 to 3500 Oe, preferably 1000 to 3500 Oe, more preferably 1500 to 3500 Oe; a squareness (residual magnetic flux density Br/saturation magnetic flux density Bm) of ordinarily 0.85 to 0.95, preferably 0.86 to 0.95, more preferably 0.87 to 0.95; a gloss (of the coating film) of ordinarily 190 to 300%, preferably 200 to 300%, more preferably 210 to 300%; a surface roughness Ra (of the coating film) of ordinarily not more than 12.0 nm, preferably 1.0 to 11.0 nm, more preferably 2.0 to 10.0 nm, even more preferably 2.0 to 9.0 nm, most preferably 2.0 to 8.0 nm; a Young's modulus (relative value to a commercially available video tape: AV T-120 produced by Victor Company of Japan, Limited) of ordinarily not less than 130, preferably not less than 132; and a linear adsorption coefficient (of the coating film) of ordinarily 1.10 to 2.00 μm⁻¹, preferably 1.20 to 2.00 μm⁻¹. As to the durability, the running durability is ordinarily not less than 11 minutes, preferably not less than 15 minutes, more preferably not less than 20 minutes. In case using the magnetic iron-based metal particles containing Al as magnetic particles for the magnetic recording layer, the running durability is ordinarily not less than 18 minutes, preferably not less than 20 minutes, more preferably not less than 22 minutes. Also, the scratch resistance is ordinarily A or B, preferably A, when evaluated into four ranks: A, B, C and D.

The corrosiveness represented by a percentage (%) of change in the coercive force is ordinarily not more than 10.0%, preferably not more than 9.5%, more preferably not more than 8.0%, and the corrosiveness represented by a percentage (%) of change in the saturation magnetic flux density Bm is ordinarily not more than 10.0%, preferably not more than 9.5%, more preferably not more than 8.0%.

What is an important in the present invention is the fact that when the high-purity acicular hematite particles containing 0.05 to 50 wt % of aluminum (calculated as Al) within the particles, which have an average major axial diameter of not more than 0.3 μm, a pH value of not less than 8, which contain soluble sodium salts of not more than 300 ppm soluble sodium (calculated as Na) and soluble sulfates of not more than 150 ppm soluble sulfate (calculated as SO₄) are used as the non-magnetic particles for a non-magnetic undercoat layer, it is possible to enhance the strength of the substrate and the surface smoothness of the non-magnetic undercoat layer owing to the excellent dispersibility of the particles into a binder resin, and that when a magnetic recording medium is formed by using the non-magnetic undercoat layer, it is possible to reduce the light transmittance, to enhance the strength and to make the surface of the magnetic recording layer more smooth.

The reason why the strength of the substrate is enhanced and the surface of the non-magnetic undercoat layer is made more smooth is considered to be as follows. Since the binder resin adsorptivity of the acicular hematite particles containing aluminum within the particles in the vehicle is enhanced, as will be shown in later-described examples, the degree of adhesion of the acicular hematite particles in the non-magnetic undercoat layer or the non-magnetic undercoat layer itself to the non-magnetic substrate is enhanced. Since it is possible to sufficiently remove the soluble sodium and the soluble sulfate, which agglomerate hematite particles by firmly crosslinking, by washing the particles with water, the agglomerates are separated into substantially discrete particles, so that acicular hematite particles having an excellent dispersion in the vehicle are obtained.

This fact will be explained in the following. The goethite particles as the starting material are produced by various methods, as described above. When the material for producing acicular goethite particles is ferrous sulfate in any method, a large amount of sulfate [SO₄ ⁻⁻] naturally exists in the goethite suspension.

Especially, when goethite particles are produced from an acidic solution, since water-soluble sulfate such as Na₂SO₄ is simultaneously produced and an alkali metal such as K⁺, NH₄ ⁺ and Na⁺ are contained in the goethite suspension, a deposit containing an alkali metal and a sulfate is easily produced. This deposit is represented by RFe₃(SO₄) (OH)₆ (R=K⁺, NH₄ ⁺, Na⁺). Such a deposit is a slightly soluble sulfuric acid-containing salt and cannot be removed by an ordinary water washing method. This slightly soluble salt becomes a soluble sodium salt or a soluble sulfate in the next heat-treatment step. The soluble sodium salt and soluble sulfate are firmly combined with the interiors or the surfaces of the acicular hematite particles by a sintering preventive, which is essential for preventing the deformation of the acicular hematite particles and sintering between particles in the heat-treatment at a high temperature for the densification of the particles and which is crosslinking the acicular hematite particles. In this manner, agglomeration between acicular hematite particles becomes further firmer. As a result, the soluble sulfate and the soluble sodium salt, especially, imprisoned in the interiors of the particles or the agglomerates become very difficult to remove by an ordinary water washing method.

When acicular goethite particles are produced in an aqueous alkali solution by using ferrous sulfate and sodium hydroxide, Na₂SO₄ is simultaneously produced as a sulfate and NaOH exists in the mother liquor. Since they are both soluble, if the acicular goethite particles are adequately washed with water, Na₂SO₄ and NaOH ought to be removed. However, since the crystallinity of acicular goethite particles is generally small, the water-washing effect is poor, and when the particles are washed with water by an ordinary method, the particles still contain water-soluble contents such as a soluble sulfate [SO₄ ⁻⁻] and a soluble sodium salt [Na⁺]. The water-soluble contents are firmly combined with the interiors or the surfaces of the acicular hematite particles by the sintering preventive which is crosslinking the particles, as described above, and the agglomeration between acicular hematite particles becomes further firmer. As a result, the soluble sulfate and the soluble sodium salt, especially, imprisoned in the interiors of the particles or the agglomerates become very difficult to remove by an ordinary water washing method.

It is considered that when the hematite particles in which the soluble sodium salt and the soluble sulfate are firmly combined with the interiors or the surfaces of the particles via the soluble sintering preventive, as described above, are pulverized by a wet-process so as to deagglomerate coarse particles, and heat-treated in the aqueous alkali solution having a pH value of not less than 13 at a temperature of not less than 80° C., the aqueous alkali solution sufficiently permeates into the interiors of the hematite particles, so that the binding strength of the sintering preventive which is firmly combined with the interiors and the surfaces of the particles, and the interiors of the agglomerates is gradually weakened, and the crosslinking is dissociated from the interiors and the surfaces of the particles and the interiors of the agglomerates, and simultaneously, the water-soluble sodium salt and the water-soluble sulfate are easily removed by water washing.

What is also important in the present invention is the fact that since the particles having a pH value of not less than 8, and containing soluble sodium salts of not more than 300 ppm soluble sodium (calculated as Na) and soluble sulfates of not more than 150 ppm soluble sulfate (calculated as SO₄) are used as the non-magnetic particles for the non-magnetic undercoat layer, it is possible to suppress the deterioration in the magnetic properties which is caused by the corrosion of the acicular magnetic iron-based metal particles dispersed in the magnetic recording layer.

It is considered that the deterioration in the magnetic properties which is caused by the corrosion of the acicular magnetic iron-based metal particles dispersed in the magnetic recording layer is suppressed because the contents of the soluble sodium salt and the soluble sulfate, which accelerate the corrosion of a metal, in the acicular hematite particles are small and the pH value of the hematite particles themselves is as high as not less than 8.

Actually, it is confirmed that a progress of corrosion of acicular magnetic iron-based metal particles was suppressed by a synergistic effect of a small soluble content and a pH value of not less than 8, from the fact that the advantages of the present invention was not attained in any of the cases of (i) heat-treating the hematite particles after wet-pulverization in a slurry with the pH value adjusted to less than 13 at a temperature of not less than 80° C., (ii) heat-treating the hematite particles in a slurry with the pH value adjusted to not less than 13 at a temperature of less than 80° C., and (iii) heat-treating the hematite particles containing coarse particles without being pulverized by a wet-process in a slurry with the pH value adjusted to not less than 13 at a temperature of not less than 80° C., as shown in later-described examples and comparative examples.

In addition, what is still another important in the present invention is that the surfaces of the magnetic recording layer and the magnetic recording medium of the present invention have an excellent durability.

The reason why the durability of the surfaces of the magnetic recording layer and the magnetic recording medium is enhanced is not clear yet, but it is considered that it is due to the effect of using the acicular hematite particles containing aluminum uniformly within the particles, having a pH value of not less than 8 and containing a small amount of soluble sodium salt and soluble sulfate as the non-magnetic particles. More specifically, it is considered that since the resin adsorptivity of the acicular hematite particles containing aluminum uniformly within the particles in the vehicles are enhanced due to the use of the above-described particles, as will be shown in later-described examples, the degree of adhesion of the acicular hematite particles in the non-magnetic undercoat layer or the non-magnetic undercoat layer itself to the non-magnetic substrate is enhanced.

When the acicular hematite particles of the present invention are used as the non-magnetic particles containing aluminum substantially uniformly within the particles for a non-magnetic undercoat layer, it is possible to produce a non-magnetic undercoat layer excellent in the strength of the substrate and the surface smoothness, and when a magnetic medium is produced by using the non-magnetic undercoat layer, it is possible to provide a magnetic medium having a small light transmittance, a smooth surface, a high strength and an excellent durability. That is, the acicular hematite particles are preferable as the non-magnetic particles for a non-magnetic undercoat layer of a high-density magnetic recording medium.

Especially, the magnetic medium of the present invention having a non-magnetic undercoat layer using the hematite particles of the present invention has a small light transmittance, a smooth surface, a high strength and an excellent durability and it is capable of suppressing the deterioration in the magnetic properties caused by a corrosion of the acicular magnetic iron-based metal particles in the magnetic recording layer. That is, the magnetic medium is preferable as a high-density magnetic medium.

Furthermore, due to the synergistic effect of using the acicular non-magnetic particles containing aluminum uniformly within the particles as the non-magnetic particles for the non-magnetic undercoat layer, and using the acicular magnetic iron-based metal particles containing aluminum as the magnetic particles for the magnetic recording layer, the durability is more excellent. That is, the magnetic medium is preferable as a high-density magnetic medium.

EXAMPLES

The present invention is described in more detail by Examples and Comparative Examples, but the Examples are only illustrative and, therefore, not intended to limit the scope of this invention.

Various properties of the lithium-iron oxide particles produced according to the present invention were evaluated by the following methods.

(1) The residue on sieve after the wet-pulverization was obtained by measuring the concentration of the slurry after pulverization by a wet-process in advance, and determining the quantity of the solid content on the sieve remaining after the slurry equivalent to 100 g of the solid content was passed through the sieve of 325 meshes (mesh size: 44 μm).

(2) The average major axial diameter and the average minor axial diameter of the particles are expressed by the average values of 350 particles measured in the photograph obtained by magnifying an electron micrograph (×30000) by 4 times in the vertical and horizontal directions, respectively. The aspect ratio is the ratio of the average major axial diameter and the average minor axial diameter.

(3) The geometrical standard deviation (σG) of particle size distribution of the major axial diameter was obtained by the following method. The major axial diameters of the particles were measured from the magnified electron microphotograph in the above-mentioned (2). The actual major axial diameters of the particles and the number of particles were obtained from the calculation on the basis of the measured values. On logarithmico-normal probability paper, the major axial diameters were plotted at regular intervals on the abscissa-axis and the accumulative number of particles belonging to each interval of the major axial diameters was plotted by percentage on the ordinate-axis by a statistical technique. The major axial diameters corresponding to the number of particles of 50% and 84.13%, respectively, were read from the graph, and the geometrical standard deviation (σg) was measured from the following formula:

Geometrical standard deviation (σg)={major axial diameter (μm) corresponding to 84.13% under integration sieve}/{major axial diameter (geometrical average diameter) corresponding to 50% under integration sieve}.

The smaller the geometrical standard deviation, the more excellent the particle size distribution of the major axial diameters of the particles.

(4) The specific surface area is expressed by the value measured by a BET method.

(5) The decree of denseness of the particles is represented by S_(BET)/S_(TEM) as described above. S_(BET) is a specific surface area measured by the above-described BET method. S_(TEM) is a value calculated from the average major axial diameter d cm and the average minor axial diameter w cm measured from the electron microphotograph described in (2) on the assumption that a particle is a rectangular parallellopiped in accordance with the following formula:

S _(TEM)(m ²/g)={(4·d·w+2w ²)/(d·w ²·ρ_(p))×10⁻⁴

wherein ρ_(p) is the true specific gravity of the hematite particles, and 5.2 g/cm³ was used.

Since S_(TEM) is a specific surface area of a particle having a smooth surface without any dehydration pore within or on the surface thereof, the closer S_(BET)/S_(TEM) of particles is to 1, it means, the smoother surface the particles have without any dehydration pore within or in the surface thereof, in other words, the particles are high-density particles.

(6) The content of each of Co, Al, Ti, P, Si, B and Nd was measured from fluorescent X-ray analysis.

(7) The pH value of the particles was measured in the following method. 5 g of the sample was weighed into a 300-ml triangle flask, and 100 ml of pure water was added. The suspension was heated and after keeping the boiled state for 5 minutes, it was corked and left to cool to an ordinary temperature. After adding pure water which was equivalent to the pure water lost by boiling, the flask was corked again, shaken for 1 minute, and left to stand for 5 minutes. The pH value of the supernatant obtained was measured in accordance JIS Z 8802-7.

(8) The contents of soluble sodium salts and soluble sulfates were measured by measuring the Na content and SO₄ ²⁻ content in the filtrate obtained by filtering the supernatant liquid produced for the measurement of pH value which is described above through filter paper No. 5C., by using an Inductively Coupled Plasma Emission Spectrophotometer (manufactured by Seiko Instruments and Electronics, Ltd.).

(9) The viscosity of the coating film composition was obtained by measuring the viscosity of the coating film composition at 25° C. at a shear rate D of 1.92 sec⁻¹ by using an E type viscometer EMD-R (manufactured by Tokyo Keiki, Co., Ltd.).

(10) The resin adsorptivity of the particles represents the degree at which a resin is adsorbed to the particles. The closer to 100 the value obtained in the following manner, the better.

The resin adsorption Wa was first obtained. 20 g of particles and 56 g of a mixed solvent (27.0 g of methyl ethyl ketone, 16.2 g of toluene, and 10.8 g of cyclohexanone) with 2 g of a vinyl chloride-vinyl acetate copolymer resin having a sodium sulfonate group dissolved therein were charged into a 100-ml polyethylene bottle together with 120 g of 3 mmφ steel beads. The particles and the solvent were mixed and dispersed by a paint shaker for 60 minutes.

Thereafter, 50 g of the coating film composition was taken out, and charged into a 50-ml settling cylinder. The solid content was separated from the solvent portion by the centrifugalization at a rate of 10000 rpm for 15 minutes. The concentration of the solid resin content contained in the solvent portion was determined by a gravimetric method and the resin content existing in the solid portion was determined by deducting the obtained resin content from the amount of the resin sharged as the resin adsorption Wa (mg/g) to the particles.

The total quantity of separated solid content was taken into a 100 ml-tall beaker, and 50 g of a mixed solvent (25.0 g of methyl ethyl ketone, 15.0 g of toluene, and 10.0 g of cyclohexanone) was added thereto. The obtained mixture was to ultrasonic dispersion for 15 minutes, and the thus-obtained suspension was charged into a 50-ml settling cylinder. The solid content was separated from the solvent portion by centrifuging them at a rate of 10000 rpm for 15 minutes. The concentration of the solid resin content contained in the solvent portion was measured so as to determine the resin content dissolved from the resin which had been adsorbed to the particle surfaces into the solvent phase.

The process from the step of taking the solid content into the 100 ml-tall beaker to the determination of the resin content dissolved into the solvent phase was repeated twice. The total quantity We (mg/g) of resin content dissolved into the solvent phase in the three cycles was obtained, and the value calculated in accordance with the following formula is expressed as the resin adsorptivity T(%):

T(%)=[(Wa−We)/Wa]×100.

The higher T value, the firmer the resin adsorption to the particles surfaces in the vehicle and the more favorable.

(11) The gloss of the surface of the coating film of each of the non-magnetic undercoat layer and the magnetic recording layer was measured at an angle of incidence of 45° by a glossmeter UGV-5D (manufactured by Suga Shikenki, Co., Ltd.).

(12) The surface roughness Ra is expressed by the average value of the center-line average roughness of the profile curve of the surface of the coating film by using “Surfcom-575A” (manufactured by Tokyo Seimitsu Co., Ltd.).

(13) The durability of the magnetic medium was evaluated by the following running durability and the scratch resistance.

The running durability was evaluated by the actual operating time under the conditions that the load was 200 gw and the relative speed of the head and the tape was 16 m/s by using “Media Durability Tester MDT-3000” (manufactured by Steinberg Associates) . The longer the actual operating time, the higher the running durability.

The scratch resistance was evaluated by observing through the microscope the surface of the magnetic tape after running and visually judging the degree of scratching. Evaluation was divided into the following four ranks.

A: No scratch

B: A few scratches

C: Many scratches

D: A great many scratches

(14) The strength of the coating film was expressed the Young's modulus obtained by “Autograph” (produced by Shimazu Seisakusho Ltd.). The Young's modulus was expressed by the ratio of the Young's modulus of the coating film to that of a commercially available video tape “AV T-120” (produce by Victor Company of Japan, Limited). The higher the relative value, the more favorable.

(15) The magnetic properties were measured under an external magnetic field of 10 kOe by “Vibration Sample Magnetometer VSM-3S-15 (manufactured by Toei Kogyo, Co., Ltd.)”.

(16) The light transmittance is expressed by the linear adsorption coefficient measured by using “Photoelectric Spectrophotometer UV-2100” (manufactured by Shimazu Seisakusho, Ltd.). The linear adsorption coefficient is defined by the following formula, and the larger the value, the more difficult it is for the magnetic sheet to transmit light:

Linear adsorption coefficient (μm⁻¹)={1n(1/t)}/FT wherein represent a light transmittance (−) at λ=900 nm, and FT represents thickness (μm) of the coating film composition of the film used for the measurement.

(17) The thickness of each of the non-magnetic substrate, the non-magnetic undercoat layer and the magnetic recording layer constituting the magnetic recording medium was measured in the following manner by using a Digital Electronic Micrometer R351C (manufactured by Anritsu Corp.) The thickness (A) of a non-magnetic substrate was first measured. Similarly, the thickness (B) (B=the sum of the thicknesses of the non-magnetic substrate and the non-magnetic undercoat layer) of a substrate obtained by forming a non-magnetic undercoat layer on the non-magnetic substrate was measured. Furthermore, the thickness (C) (C=the sum of the thicknesses of the non-magnetic substrate, the non-magnetic undercoat layer and the magnetic recording layer) of a magnetic recording medium obtained by forming a magnetic recording layer on the non-magnetic undercoat layer was measured. The thickness of the non-magnetic undercoat layer is expressed by B-A, and the thickness of the magnetic recording layer is expressed by C-B.

(18) The chance in the magnetic properties with passage of time of a magnetic recording medium caused by the corrosion of the magnetic iron-based metal particles was examined as follows.

The magnetic recording medium was allowed to stand in an environment of a temperature of 60° C. and a relative humidity of 90% for 14 days, and the coercive force and the saturation magnetic flux density were measured before and after standing. A change in each characteristic was divided by the value before standing, and represented by percentage as a percentage of change.

(19) The light transmittance of a magnetic sheet is expressed by the linear adsorption coefficient measured by using “Photoelectric Spectrophotometer UV-2100” (manufactured by Shimazu Seisakusho, Ltd.), The linear adsorption coefficient is defined by the following formula:

Linear adsorption coefficient (μm ⁻¹)={1n(1/t)}/FT

wherein t represents light transmittance (−) at λ=900 nm, and FT represents thickness (μm) of the coating film composition of the film used for the measurement.

The larger the value, the more difficult it is for the magnetic sheet to transmit light.

As a blank for measuring the linear adsorption coefficient, the same non-magnetic base film as that of the above-mentioned magnetic sheet, was used.

Example 1 Production of Spindle-shaped Hematite Particles

1200 g of spindle-shaped goethite particles containing 0.61 wt % of aluminum (calculated as Al) uniformly within the particles (average major axial diameter: 0.153 μm, average minor axial diameter: 0.0196 μm, aspect ratio: 7.80, BET specific surface area: 175.2 m²/g, content of soluble sodium salts: 1130 ppm soluble sodium (calculated as Na), content of soluble sulfates: 522 ppm soluble sulfate (calculated as SO₄), pH value of the particles: 7.9, geometrical standard deviation: 1.32), obtained from an aqueous ferrous sulfate solution, an aqueous aluminum sulfate solution and an aqueous sodium carbonate solution according to the method (B) was suspended in water so as to obtain a slurry, and the concentration of the solid content was adjusted 8 g/liter. 150 liter of the slurry was heated to 60° C. and the pH value of the slurry was adjusted to 9.0 by adding a 0.1-N aqueous NaOH solution.

To the alkali slurry was gradually added 30.0 g of #3 water glass as a sintering preventive, and after the end of addition, the obtained mixture was aged for 60 minutes. The pH value of the slurry was then adjusted to 5.8 by adding a 0.1-N acetic acid solution. Thereafter, the particles were filtered out, washed with water, dried and pulverized by an ordinary method, thereby producing spindle-shaped goethite particles coated with a silicon oxide and containing aluminum uniformly within the particles. The SiO₂ content in the spindle-shaped goethite particles was 0.72 wt %.

1000 g of the spindle-shaped goethite particles obtained were charged into a stainless steel rotary furnace, and heat-treated and dehydrated in the air at 300° C. for 60 minutes while rotating the furnace, to obtain low-density spindle-shaped hematite particles containing aluminum uniformly within the particles. The thus-obtained low-density spindle-shaped hematite particles had an average major axial diameter of 0.115 μm, an average minor axial diameter of 0.0177 μm, an aspect ratio of 6.50, a BET specific surface area (S_(BET)) of 187.3 m²/g, and a S_(BET)/S_(TEM) value of densification of 4.00. The goethite particles contained soluble sodium salts of 1361 ppm soluble sodium (calculated as Na) and soluble sulfates of 568 ppm soluble sulfate (calculated as SO₄). The Al content was 0.67 wt %, the pH value of the particles was 7.8 and the geometrical standard deviation thereof was 1.34. The SiO₂ content in the low-density spindle-shaped hematite particles was 0.81 wt %.

650 g of the low-density spindle-shaped hematite particles were then charged into a ceramic rotary furnace, and heat-treated in the air at 640° C. for 20 minutes while rotating the furnace so as to conduct the sealing of dehydration pores. The thus-obtained high-density spindle-shaped hematite particles containing aluminum uniformly within the particles had an average major axial diameter of 0.110 μm, an average minor axial diameter of 0.0186 μm, an aspect ratio of 5.91, a BET specific surface area (S_(BET)) of 54.6 m²/g, and a S_(BET)/S_(TEM) value of densification of 1.22. The hematite particles contained soluble sodium salts of 3553 ppm soluble sodium (calculated as Na) and soluble sulfates of 3998 ppm soluble sulfate (calculated as SO₄). The pH value of the particles was 5.8 and the geometrical standard deviation was 1.36. The SiO₂ content in the hematite particles was 0.82 wt %. The resin adsorptivity thereof was 23.8%.

After 800 g of the high-density spindle-shaped hematite particles obtained were roughly pulverized by a Nara mill in advance, the obtained particles were charged into 4.7 1 of pure water and peptized by a homomixer (manufactured by Tokushu-kika Kogyo, CO., Ltd.) for 60 minutes.

The slurry of the high-density spindle-shaped hematite particles obtained was then mixed and dispersed for 3 hours at an axial rotation frequency of 2000 rpm while being circulated by a horizontal SCM (Dispermat SL, manufactured by S.C. Adichem, CO., Ltd.). The spindle-shaped hematite particles in the slurry remaining on a sieve of 325 meshes (mesh size: 44 μm) was 0% by weight.

The concentration of the high-density spindle-shaped hematite particles in the slurry was adjusted to 100 g/liter, and 6N-aqueous NaOH solution was added to 7 liter of the slurry under stirring so as to adjust the pH value to 13.3. The slurry was then heated to 95° C. under stirring, and was held for 3 hours at 95° C.

The slurry was then washed with water by a decantation method and the pH value of the slurry was adjusted to 10.5. When the concentration of the slurry at this point was checked so as to ensure the accuracy, it was 98 g/liter.

2 liter of the slurry washed with water was filtered through a Buchner filter, and pure water was passed until the electric conductivity of the filtrate became not more than 30 μs. The particles were then dried by an ordinary method and pulverized so as to obtain the target spindle-shaped hematite particles. The spindle-shaped hematite particles obtained contained 0.67 wt % of aluminum (calculated as Al) uniformly within the particles, and had an average major axial diameter of 0.110 μm, a minor axial diameter of 0.0185 μm, an aspect ratio of 5.95, a geometric standard deviation ρg of particle size (major axial diameter) of 1.35, a BET specific surface (S_(BET)) of 54.0 m²/g, a S_(BET)/S_(TEM) value of densification of 1.20 and a pH value of the particles of 9.0. The spindle-shaped hematite particles contained soluble sodium salts of 138 ppm soluble sodium (calculated as Na) and soluble sulfates of 35 ppm soluble sulfate (calculated as SO₄). The resin adsorptivity thereof was 79.8%.

Example 2 Production of a Non-magnetic Undercoat Layer

12 g of the spindle-shaped hematite particles containing 0.67 wt % of aluminum (calculated as Al) uniformly within the particles obtained in the Example 1 were mixed with a binder resin solution (30 wt % of vinyl chloride-vinyl acetate copolymer resin having a sodium sulfonate group and 70 wt % of cyclohexanone) and cyclohexanone, and the mixture (solid content: 72 wt %) obtained was kneaded by a plasto-mill for 30 minutes.

The thus-obtained kneaded material was charged into a 140 ml-glass bottle together with 95 g of 1.5 mmφ glass beads, a binder resin solution (30 wt % of polyurethane resin having a sodium sulfonate group and 70 wt % of a solvent (methyl ethyl ketone:toluene=1:1)), cyclohexanone, methyl ethyl ketone and toluene, and the obtained mixture was mixed and dispersed by a paint shaker for 6 hours to obtain a coating film composition.

The thus-obtained coating film composition containing hematite particles was as follows:

Spindle-shaped hematite particles 100 parts by weight Vinyl chloride-vinyl acetate 10 parts by weight copolymer resin having a sodium sulfonate group Polyurethane resin having a 10 parts by weight sodium sulfonate group Cyclohexanone 44.6 parts by weight Methylethyl ketone 111.4 parts by weight Toluene 66.9 parts by weight

The viscosity of the obtained coating film composition was 384 cP. The coating film composition obtained containing hematite particles was applied to a polyethylene terephthalate film of 12 μm thick to a thickness of 55 μm by an applicator, and the film was then dried, thereby forming a non-magnetic undercoat layer. The thickness of the non-magnetic undercoat layer was 3.5 μm.

The gloss of the coating film of the non-magnetic undercoat layer was 206%, the surface roughness Ra was 5.9 nm, and the Young's modulus (relative value) was 121.

Production of a Magnetic Recording Layer

12 g of acicular magnetic iron-based metal particles (average major axial diameter: 0.11 μm, average minor axial diameter: 0.018 μm, aspect ratio: 6.10, coercive force: 1880 Oe, saturation magnetization: 128 emu/g), 1.2 g of a polishing agent (AKR-30: trade name, produced by Sumitomo Chemical Co., Ltd.), 0.12 g of carbon black (#3250B, trade name, produced by Mitsubishi Chemical Corp.), a binder resin solution (30 wt % of vinyl chloride-vinyl acetate copolymer resin having a sodium sulfonate group and 70 wt % of cyclohexanone) and cyclohexanone were mixed to obtain a mixture (solid content: 78 wt %). The mixture was further kneaded by a plasto-mill for 30 minutes to obtain a kneaded material.

The thus-obtained kneaded material was charged into a 140 ml-glass bottle together with 95 g of 1.5 mmφ glass beads, a binder resin solution (30 wt % of polyurethane resin having a sodium sulfonate group and 70 wt % of a solvent (methyl ethyl ketone:toluene=1:1)), cyclohexanone, methyl ethyl ketone and toluene, and the mixture was mixed and dispersed by a paint shaker for 6 hours.

The thus-obtained magnetic coating film composition was as follows:

Iron-based alloy particles 100 parts by weight Vinyl chloride-vinyl acetate 10 parts by weight copolymer resin having a sodium sulfonate group Polyurethane resin having a 10 parts by weight sodium sulfonate group Polishing agent (AKP-30) 10 parts by weight Carbon black (#3250B) 3.0 parts by weight Lubricant (myristic acid:butyl 3.0 parts by weight stearate = 1:2) Hardening agent (polyisocyanate) 5.0 parts by weight Cyclohexanone 65.8 parts by weight Methyl ethyl ketone 164.5 parts by weight Toluene 98.7 parts by weight

The magnetic coating film composition obtained was applied to the non-magnetic undercoat layer to a thickness of 15 μm by an applicator, and the magnetic recording medium obtained was oriented and dried in a magnetic field, and then calendered. The magnetic recording medium was then subjected to a curing reaction at 60° C. for 24 hours, and thereafter slit into a width of 0.5 inch, thereby obtaining a magnetic tape. The thickness of the magnetic recording layer was 1.1 μm.

The magnetic tape obtained had a coercive force of 1960 Oe, a squareness (Br/Bm) of 0.87, a gloss of 235%, a surface roughness Ra of 6.0 nm, a Young's modulus (relative value) of 133, a linear absorption coefficient of 1.21, a running durability of 25.6 minutes, and a scratch resistance of A. Changes in the coercive force and the saturation magnetic flux density Bm with passage of time were 5.0%, and 4.2%, respectively.

Examples 3 to 17, Comoarative Examples 1 to 15 Types of Acicular Goethite Particles

The precursors 1 to 8 shown in Table 1 were used as the precursors for producing acicular hematite particles.

Production of Low-density Acicular Hematite Particles

Low-density acicular hematite particles were obtained in the same way as in Example 1 except for varying the kind of acicular goethite particles as the precursors, the kind and amount of sintering preventive, and heating and dehydration temperature and time. The particles obtained in Comparative Example 4 were goethite particles.

The main producing conditions and various properties are shown in Tables 2 to 5.

Examples 18 to 32, Comparative Examples 16 to 29 Production of High-density Acicular Hematite Particles

High-density acicular hematite particles were obtained in the same way as in Example 1 except for varying the kind of low-density hematite particles, and the heating temperature and time for densification.

The main producing conditions and various properties are shown in Tables 6 and 7.

Examples 33 to 47, Comparative Examples 30 to 38 Treatment of Acicular Hematite Particles in an Acqueous Alkali Solution

Acicular hematite particles were obtained in the same way as in Example 1 except for varying the kind of high-density acicular hematite particles, whether or not the wet-pulverization process was conduced, whether or not the heat-treatment in the aqueous alkali solution was conducted, the pH value of the slurry, and the heating time and temperature.

The main producing conditions and various properties are shown in Tables 8 to 11.

Example 48 Surface Coating of Spindle-shaped Hematite Particles

The concentration of the slurry having a pH value 10.5 which was obtained in Example 33 by washing the particles in an aqueous alkali solution after heat-treatment with water by a decantation method was 98 g/liter. 5 liter of the slurry was re-heated to 60° C., and 907 ml (equivalent to 5.0 wt % (calculated as Al) based on the spindle-shaped hematite particles) of a 1.0-N NaAlO₂ solution was added to the slurry, and the mixture was held for 30 minutes. Thereafter, the pH value of the mixture was adjusted to 8.3 by using acetic acid. The particles were then filtered out, washed with water, dried and pulverized in the same way as in Example 1, thereby obtaining spindle-shaped hematite particles coated with a coating material.

The main producing conditions and various properties are shown in Tables 12 and 13.

Examples 49 to 62

Acicular hematite particles coated with a coating material were obtained in the same way as in Example 48 except for varying the kind of acicular hematite particles, and the kind and the amount of surface treating material.

The main producing conditions and various properties are shown in Table 12 and 13.

Examples 63 to 92, Comparative Examples 39 to 54 Production of a Non-magnetic Undercoat Layer

A non-magnetic undercoat layer was obtained in the same way as in Example 2 by using the acicular hematite particles obtained in Examples 33 to 62, Comparative Examples 1, 3, 16 to 19, 24 and 30 to 38.

The main producing conditions and various properties are shown in Tables 14 to 16.

Examples 93 to 122, Comparative Examples 55 to 70 Production of a Magnetic Recording Medium Using Magnetic Iron-based Metal Particles

A magnetic recording medium using magnetic iron-based metal particles was obtained in the same way as in Example 2 except for varying the kind of non-magnetic undercoat layer obtained in Examples 63 to 92 and Comparative Examples 39 to 54 and the kind of acicular magnetic iron-based metal particles.

The main producing conditions and various properties are shown in Tables 17 to 19.

Example 123 Production of Spindle-shaped Hematite Particles

1200 g of spindle-shaped goethite particles containing 0.83 wt % of aluminum (calculated as Al) uniformly within the particles (average major axial diameter: 0.178 μm, average minor axial diameter: 0.0225 μm, aspect ratio: 7.91, BET specific surface area: 160.3 m²/g, soluble sodium salts: 1232 ppm soluble sodium (calculated as Na), soluble sulfates: 621 ppm soluble sulfate (calculated as SO₄), pH value of the particles: 6.7, geometrical standard deviation: 1.33) obtained from an aqueous ferrous sulfate solution, an aqueous aluminum sulfate solution and an aqueous sodium carbonate solution by the method (B) was suspended in water so as to obtain a slurry, and the concentration of the solid content was adjusted to 8 g/liter. 150 liter of the slurry was heated to 60° C. and the pH value of the slurry was adjusted to 9.0 by adding a 0.1-N aqueous NaOH solution.

To the alkali slurry was gradually added 36.0 g of #3 water glass as a sintering preventive, and after the end of addition, the mixture was aged for 60 minutes. The pH value of the slurry was then adjusted to 6.0 by adding a 0.5-N acetic acid solution. Thereafter, the particles were filtered out, washed with water, dried and pulverized by an ordinary method, thereby producing spindle-shaped goethite particles coated with a silicon oxide and containing aluminum uniformly within the particles. The SiO₂ content in the spindle-shaped goethite particles was 0.86 wt %.

1000 g of the spindle-shaped goethite particles obtained were charged into a stainless steel rotary furnace, and heat-treated and dehydrated in the air at 350° C. for 30 minutes while rotating the furnace, to obtain low-density spindle-shaped hematite particles. The thus-obtained low-density spindle-shaped hematite particles had an average major axial diameter of 0.134 μm, an average minor axial diameter of 0.0194 μm, an aspect ratio of 6.91, a BET specific surface area (S_(BET)) of 168.3 m²/g, and a S_(BET)/S_(TEM) value of densification of 3.96. The goethite particles contained soluble sodium salts of 1123 ppm soluble sodium (calculated as Na) and soluble sulfates of 465 ppm soluble sulfate (calculated as SO₄). The Al content was 0.91 wt %, the pH value of the particles was 6.3 and the geometrical standard deviation was 1.34. The SiO₂ content in the low-density spindle-shaped hematite particles was 0.94 wt %.

900 g of the low-density spindle-shaped hematite particles were then charged into a ceramic rotary furnace, and heat-treated in the air at 630° C. for 30 minutes while rotating the furnace so as to conduct the sealing of dehydration pores. The thus-obtained high-density spindle-shaped hematite particles containing aluminum uniformly within the particles had an average major axial diameter of 0.129 μm, an average minor axial diameter of 0.0206 μm, an aspect ratio of 6.26, a BET specific surface area (S_(BET)) of 46.6 m²/g, and a S_(BET)/S_(TEM) value of densification of 1.16. The hematite particles contained soluble sodium salts of 2864 ppm soluble sodium (calculated as Na) and soluble sulfates of 2956 ppm soluble sulfate (calculated as SO₄). The pH value of the particles was 5.4 and the geometrical standard deviation was 1.36. The SiO₂ content in the hematite particles was 0.94 wt %. The resin adsorptivity thereof was 21.6%.

After 800 g of the high-density spindle-shaped hematite particles obtained were roughly pulverized by a Nara mill in advance, the obtained spindle-shaped hematite particles were charged into 4.7 liter of pure water and peptized by a homomixer (manufactured by Tokushu-kika Kogyo, CO., Ltd.) for 60 minutes.

The slurry of the high-density spindle-shaped hematite particles obtained was then mixed and dispersed for 3 hours at an axial rotation frequency of 2000 rpm while being circulated by a horizontal SGM (Dispermat SL, manufactured d by S.C. Adichem, CO., Ltd.). The spindle-shaped hematite particles in the slurry remaining on a sieve of 325 meshes (mesh size: 44 μm) was 0% by weight.

The concentration of the high-density spindle-shaped hematite particles in the slurry was adjusted to 100 g/liter, and a 6N-aqueous NaOH solution was added to 7 liter of the slurry under stirring so as to adjust the pH value to 13.3. The slurry was then heated to 95° C. under stirring, and was held for 3 hours at 95° C.

The slurry was then washed with water by a decantation method and the pH value of the slurry was adjusted to 10.5. When the concentration of the slurry at this point was checked so as to ensure the accuracy, it was 96 g/liter.

2 liter of the slurry washed with water was filtered through a Buchner filter, and the pure water was passed until the electric conductivity of the filtrate became not more than 30 μs. The particles were then dried by an ordinary method and pulverized so as to obtain the target spindle-shaped hematite particles. The spindle-shaped hematite particles obtained contained 0.91 wt % of aluminum (calculated as Al) uniformly within the particles, and had an average major axial diameter of not more than 0.128 μm, a minor axial diameter of 0.0206 μm, a specific ratio of 6.21, a geometric standard deviation ρg of particle size (major axial diameter) of 1.35, a BET specific surface (S_(BET)) of 47.1 m²/g, a S_(BET)/S_(TEM) value of densification of 1.17 and a pH value of the particles of 9.1. The spindle-shaped hematite particles contained soluble sodium salts of 112 ppm soluble sodium (calculated as Na) and soluble sulfates of 41 ppm of soluble sulfate (calculated as SO₄). The resin adsorptivity thereof was 86.3%.

Example 124 Production of a Non-magnetic Undercoat Layer

12 g of the spindle-shaped hematite particles containing 0.91 wt % of aluminum (calculated as Al) uniformly within the particles obtained were mixed with a binder resin solution (30 wt % of vinyl chloride-vinyl acetate copolymer resin having a sodium sulfonate group and 70 wt % of cyclohexanone) and cyclohexanone, and the mixture (solid content: 72 wt %) obtained was kneaded by a plasto-mill for 30 minutes.

A coating film composition was obtained in the same way as in Example 2 by using the kneaded material obtained.

The viscosity of the coating film composition obtained was 435 cP. The coating film composition obtained containing hematite particles was applied to a polyethylene terephthalate film of 12 μm thick to a thickness of 55 μm by an applicator, and the film was then dried, thereby forming a non-magnetic undercoat layer. The thickness of the non-magnetic undercoat layer was 3.4 μm. The gloss of the coating film of the non-magnetic undercoat layer was 211%, the surface roughness Ra was 6.2 nm, and the Young's modulus (relative value) was 131.

Production of a Magnetic Recording Layer

12 g of acicular magnetic iron-based metal particles (average major axial diameter: 0.104 μm, average minor axial diameter: 0.0158 μm, aspect ratio: 6.58, coercive force: 1905 Oe, saturation magnetization: 138 emu/g, geometric standard deviation: 1.35, resin adsorptivity: 80.1%), which contained 1.12 wt % of aluminum in the central portion, 2.55 wt % of aluminum in the surface layer portion, and 0.48 wt % of aluminum on the surface coating (calculated as Al), respectively, and further contained 0.36 wt % of Nd, 1.2 g of a polishing agent (AKP-30: trade name, produced by Sumitomo Chemical Co., Ltd.), 0.36 g of carbon black (#3250B, trade name, produced by Mitsubishi Chemical Corp.), a binder resin solution (30 wt % of vinyl chloride-vinyl acetate copolymer resin having a sodium sulfonate group and 70 wt % of cyclohexanone) and cyclohexanone were mixed to obtain a mixture (solid content: 78 wt %). The mixture was further kneaded by a plasto-mill for 30 minutes to obtain a kneaded material.

A magnetic tape was produced in the same way as in Example 2 by using the kneaded material obtained. The thickness of the magnetic recording layer of the magnetic tape was 1.1 μm.

The magnetic tape obtained by forming the magnetic recording layer on the non-magnetic undercoat layer had a coercive force of 1981 Oe, a squareness (Br/Bm) of 0.88, a gloss of 228%, a surface roughness Ra of 6.0 nm, a Young's modulus (relative value) of 132, a linear absorption coefficient of 1.23, a running durability of 30.0 minutes, and a scratch resistance of A.

Changes in the coercive force and the saturation magnetic flux density Bm with passage time were 3.4% and 4.5%, respectively.

Examples 125 to 133, Comoarative Examples 71 to 84 Kinds of Acicular Goethite Particles

The following starting materials (I) to (V) were prepared as the precursors for the production of acicular hematite particles. The main producing conditions and various properties are shown in Table 20.

Production of Low-density Acicular Hematite Particles

Low-density acicular hematite particles were produced in the same way as in Example 123 except for varying the kind of acicular goethite particles, the kind and amount of sintering preventive, the heating temperature and time. The particle obtained in Comparative Example 74 were goethite particles.

The main producing conditions and various properties are shown in Tables 21 to 24.

Examples 134 to 142, Comparative Examples 85 to 97 Production of High-density Acicular Hematite Particles

High-density acicular hematite particles were produced in the same way as in Example 123 except for varying the kind of low-density acicular hematite particles, and the heating temperature and time for densification.

The main producing conditions and various properties are shown in Tables 25 and 26.

Examples 143 to 151, Comparative Examples 98 to 105 Treatment of Acicular Hematite Particles in an Aqueous Alkali solution

Acicular hematite particles were obtained in the same way as in Example 123 except for varying the kind of high-density acicular hematite particles, whether or not the wet-pulverization process was conducted, whether or not the heat-treatment in the aqueous alkali solution was conducted, the pH value of the slurry, and the heating time and temperature.

The main producing conditions and various properties are shown in Tables 27 to 30.

Example 152 Surface Coating of Acicular Hematite Particles

The concentration of the slurry having a pH value 10.5 which was obtained in Example 143 by washing the particles in an aqueous alkali solution after heat-treatment with water by a decantation method was 96 g/liter. 5 liter of the slurry was re-heated to 60° C., and 533 ml (equivalent to 3.0 wt % (calculated as Al) based on the acicular hematite particles) of a 1.0-N NaAlO₂ solution was added to the slurry, and the mixture was held for 60 minutes. Thereafter, the pH value of the mixture was adjusted to 8.2 by using acetic acid. The particles were then filtered out, washed with water, dried and pulverized in the same way as in Example 123, thereby obtaining acicular hematite particles coated with a coating material.

The main producing conditions and various properties are shown in Tables 31 and 32.

Examples 153 to 160

Acicular hematite particles coated with a coating material were obtained in the same way as in Example 152 except for varying the kind of acicular hematite particles, and the kind and the amount of surface treating material.

The main producing conditions and various properties are shown in Tables 31 and 32

Examples 161 to 178, Comparative Examples 106 to 120 Production of a Non-magnetic Undercoat Layer

A non-magnetic undercoat layer was obtained in the same way as in Example 124 by using the acicular hematite particles obtained in Examples 143 to 160, acicular hematite particles as the starting material (V), and the acicular hematite particles obtained in Comparative Examples 73, 85 to 88, 93 and 98 to 105.

The main producing conditions and various properties are shown in Tables 33 and 34.

Examples 179 to 191, Comparative Examples 121 to 134 Production of a Magnetic Recording Medium

4 kinds of magnetic iron-based metal particles (a) to (d) shown in Table 35 were used.

A magnetic recording medium using magnetic iron-based metal particles was obtained in the same way as in Example 124 except for varying the kind of non-magnetic undercoat layer and the kind of acicular magnetic iron-based metal particles.

The main producing conditions and various properties are shown in Tables 36 and 37.

TABLE 1 Precursor Precursor Precursor Precursor Kind of precursors 1 2 3 4 Production of acicular goethite particles Production method B B D C Kind of Al added Aluminum Aluminum Aluminum Aluminum sulfate sulfate nitrate acetate Acicular goethite particles Average major axial 0.179 0.228 0.246 0.196 diameter (μm) Aspect ratio (−) 7.6 7.9 8.1 7.7 Geometric standard 1.35 1.32 1.30 1.38 deviation σg (−) BET specific 146.0 101.0 85.3 95.1 surface area (m²/g) Al content (wt %) 0.60 1.12 0.84 0.20 Soluble Na salt 389 453 1389 365 (ppm) Soluble sulfate 235 564 2323 890 (ppm) pH value of 7.9 7.3 6.1 5.5 particles (−) Precursor Precursor Precursor Precursor Kind of precursors 5 6 7 8 Production of acicular goethite particles Production method B B A B Kind of Al added Aluminum Aluminum Sodium Aluminum sulfate sulfate aluminate sulfate Acicular goethite particles Average major axial 0.150 0.235 0.216 0.258 diameter (μm) Aspect ratio (−) 7.4 8.4 8.8 8.6 Geometric standard 1.42 1.30 1.40 1.35 deviation σg (−) BET specific 186.4 65.6 75.1 60.6 surface area (m²/g) Al content (wt %) 0.46 2.89 4.05 0.005 Soluble Na salt 456 399 1189 325 (ppm) Soluble sulfate 367 412 268 525 (ppm) pH value of 7.1 6.8 8.4 7.0 particles (−)

(Note) PRODUCTION METHOD:

(A): A method of oxidizing a suspension having a pH value of not less than 11 and containing colloidal ferrous hydroxide particles which is obtained by adding not less than an equivalent of an alkali hydroxide solution to an aqueous ferrous salt solution, by passing an oxygen-containing gas thereinto at a temperature of not higher than 80° C.

(B): A method of producing spindle-shaped goethite particles by oxidizing a suspension containing FeCO₃ which is obtained by reacting an aqueous ferrous salt solution with an aqueous alkali carbonate solution, by passing an oxygen-containing gas thereinto after aging the suspension, if necessary.

(C): A method of growing acicular seed goethite particles by oxidizing a ferrous hydroxide solution containing colloidal ferrous hydroxide particles which is obtained by adding less than an equivalent of an alkali hydroxide solution or an alkali carbonate solution to an aqueous ferrous salt solution, by passing an oxygen-containing gas thereinto, thereby producing acicular seed goethite particles, adding not less than an equivalent of an alkali hydroxide solution to the Fe²⁺ in the aqueous ferrous salt solution, to the aqueous ferrous salt solution containing the acicular goethite seed particles, and passing an oxygen-containing gas into the aqueous ferrous salt solution.

(D): A method of growing acicular seed goethite particles by oxidizing a ferrous hydroxide solution containing colloidal ferrous hydroxide particles which is obtained by adding less than an equivalent of an alkali hydroxide solution or an alkali carbonate solution to an aqueous ferrous salt solution, by passing an oxygen-containing gas thereinto, thereby producing acicular seed goethite particles, and growing the obtained acicular seed goethite particles in an acidic or neutral region.

TABLE 2 Example 3 Example 4 Example 5 Example 6 Kind of Precursors Precursor Precursor 1 Precursor acicular in 1 2 goethite Examples particles Sintering preventive Kind #3 Water hexameta- #3 Water glass/ Phosphoric glass phosphate Phosphoric acid Soda acid Amount SiO₂: 0.75 P: 0.60 SiO₂: 1.25/ P: 1.50 added P: 1.00 (wt %) Heating and dehydration Temperature 300 350 380 350 (° C.) Time (min.) 60 60 60 60 Example 7 Example 8 Example 9 Example 10 Kind of Precursor 2 Precursor 3 Precursor 3 Precursor 4 acicular goethite particles Sintering preventive Kind Sodium hexameta- Boric acid #3 Water aluminate phosphate glass Soda Amount Al: 3.00 P: 1.20 B: 1.60 SiO₂: 1.00 added (wt %) Heating and dehydration Temperature 330 330 350 320 (° C.) Time (min.) 120 120 90 60 Example 11 Example 12 Example 13 Example 14 Kind of Precursor Precursor Precursor 5 Precursor acicular 4 5 6 goethite particles Sintering preventive Kind Phosphoric hexameta- #3 Water glass/ #3 Water acid phosphate hexameta- glass Soda phosphate soda Amount P: 1.00 P: 7.00 SiO₂: 0.75/ SiO₂: 1.50 added P: 1.25 (wt %) Heating and dehydration Temperature 300 380 350 350 (° C.) Time (min.) 30 120 90 60 Example 15 Example 16 Example 17 Kind of Precursor 6 Precursor Precursor acicular 7 7 goethite particles Sintering preventive Kind Titanyl sulfate/ hexameta- Aluminum Phosphoric acid phosphate sulfate Soda Amount Ti: 3.35 P: 1.00 Al: 3.25 added (wt %) P: 2.20 Heating and dehydration Temperature 375 310 330 (° C.) Time (min.) 60 30 60

TABLE 3 Example 3 Example 4 Example 5 Example 6 Low-density hematite particles Average major axial 0.115 0.133 0.140 0.166 diameter (μm) Average minor axial 0.0178 0.0218 0.0221 0.0263 diameter (μm) Geometric standard 1.35 1.33 1.33 1.37 deviation σg (−) Aspect ratio (−) 6.46 6.10 6.33 6.31 S_(BET) (m²/g) 187.3 150.5 160.8 143.9 S_(TEM) (m²/g) 46.6 38.2 37.6 31.6 S_(BET)/S_(TEM) (−) 4.02 3.94 4.28 4.56 Al content (wt %) 0.67 0.67 0.67 1.25 Amount of sintering SiO₂: 0.83 P: 0.66 SiO₂: 1.38 P: 1.60 preventive (wt %) P: 1.10 Soluble Na salt 1361 1897 1835 1768 (ppm) Soluble sulfate 568 1321 1189 1443 (ppm) pH value of 7.9 7.1 7.3 7.0 particles (−) Example Example 7 Example 8 Example 9 10 Low-density hematite particles Average major axial 0.168 0.204 0.206 0.147 diameter (μm) Average minor axial 0.0260 0.0291 0.0290 0.0242 diameter (μm) Geometric standard 1.36 1.41 1.40 1.35 deviation σg (−) Aspect ratio (−) 6.46 7.01 7.10 6.07 S_(BET) (m²/g) 134.8 125.9 145.0 145.9 S_(TEM) (m²/g) 31.9 28.3 28.4 34.4 S_(BET)/S_(TEM) (−) 4.23 4.45 5.11 4.24 Al content (wt %) 1.25 0.93 0.93 0.22 Amount of sintering Al: 3.24 P: 1.30 B: 1.75 SiO₂: 1.11 preventive (wt %) Soluble Na salt 1689 2567 3109 1123 (ppm) Soluble sulfate 1567 1011 980 760 (ppm) pH value of 6.8 7.9 8.3 7.8 particles (−) Example Example Example Example 11 12 13 14 Low-density hematite particles Average major axial 0.147 0.107 0.097 0.190 diameter (μm) Average minor axial 0.0240 0.0181 0.0191 0.0287 diameter (μm) Geometric standard 1.36 1.41 1.44 1.32 deviation σg (−) Aspect ratio (−) 6.13 5.91 5.08 6.62 S_(BET) (m²/g) 156.9 257.5 246.2 98.8 S_(TEM) (m²/g) 34.7 46.1 44.2 28.8 S_(BET)/S_(TEM) (−) 4.53 5.59 5.57 3.43 Al content (wt %) 0.22 0.51 0.52 3.22 Amount of sintering P: 1.09 P: 7.28 SiO₂: 0.83 SiO₂: 1.68 preventive (wt %) P: 1.36 Soluble Na salt 1324 1324 1145 876 (ppm) Soluble sulfate 689 1126 1123 888 (ppm) pH value of 8.0 6.5 6.9 6.0 particles (−) Example 15 Example 16 Example 17 Low-density hematite particles Average major axial 0.192 0.176 0.177 diameter (μm) Average minor axial 0.0278 0.0251 0.0255 diameter (μm) Geometric standard 1.32 1.36 1.37 deviation σg (−) Aspect ratio (−) 6.91 7.01 6.94 S_(BET) (m²/g) 101.8 126.8 136.9 S_(TEM) (m²/g) 29.7 32.8 32.3 S_(BET)/S_(TEM) (−) 3.43 3.86 4.23 Al content (wt %) 3.22 4.50 4.51 Amount of sintering Ti: 3.55 P: 1.11 Al: 3.58 preventive (wt %) P: 2.41 Soluble Na salt 769 1452 1562 (ppm) Soluble sulfate 658 467 576 (ppm) pH value of 6.1 8.1 8.0 particles (−)

TABLE 4 Comp. Comp. Comp. Comp. Example 1 Example 2 Example 3 Example 4 Kind of Precursors Precursors Precursors Precursors acicular in Examples in Examples in Examples in Examples goethite particles Sintering preventive Kind — — #3 Water Phosphoric glass acid Amount — — SiO₂: 1.00 P: 1.00 added (wt %) Heating and dehydration Temperature 320 350 350 — (° C.) Time (min.) 60 60 60 — Comp. Comp. Comp. Comp. Example 5 Example 6 Example 7 Example 8 Kind of Precursors Precursors Precursors Precursors acicular in Examples in Examples in Examples in Examples goethite particles Sintering preventive Kind Phosphoric Phosphoric #3 Water #3 Water acid acid glass glass Amount P: 1.25 P: 1.00 SiO₂: 1.50 SiO₂: 1.00 added (wt %) Heating and dehydration Temperature 330 310 320 350 (° C.) Time (min.) 30 30 90 60 Comp. Comp. Comp. Comp. Example 9 Example 10 Example 11 Example 12 Kind of Precursors Precursor 6 Precursor 6 Precursor 6 acicular in Examples goethite particles Sintering preventive Kind Phosphoric hexameta- #3 Water Sodium acid phosphate glass aluminate Soda Amount P: 1.00 P: 2.00 SiO₂: 1.75 Al: 1.50 added (wt %) Heating and dehydration Temperature 300 380 350 330 (° C.) Time (min.) 30 90 90 30 Comp. Comp. Comp. Example 13 Example 14 Example 15 Kind of Precursor 6 Precursor 6 Precursor 8 acicular goethite particles Sintering preventive Kind Titanyl Phosphoric Phosphoric sulfate acid acid Amount Ti: 1.00 P: 1.00 P: 1.50 added (wt %) Heating and dehydration Temperature 325 330 350 (° C.) Time (min.) 45 60 90

TABLE 5 Comp. Comp. Comp. Comp. Example 1 Example 2 Example 3 Example 4 Low-density hematite particles Average major axial 0.114 0.113 0.115 — diameter (μm) Average minor axial 0.0178 0.0177 0.0176 — diameter (μm) Geometric standard 1.35 1.33 1.33 — deviation σg (−) Aspect ratio (−) 6.40 6.38 6.53 — S_(BET) (m²/g) 187.3 150.5 160.8 — S_(TEM) (m²/g) 46.6 46.9 47.1 — S_(BET)/S_(TEM) (−) 4.02 3.21 3.42 — Al content (wt %) 0.67 0.67 0.67 — Amount of sintering — — SiO₂: 1.09 P: 1.10 preventive (wt %) Soluble Na salt 980 889 1256 — (ppm) Soluble sulfate 635 589 789 — (ppm) pH value of 7.8 6.8 6.8 — particles (−) Resin adsorptivity 15.6 — 17.6 — (%) Comp. Comp. Comp. Comp. Example 5 Example 6 Example 7 Example 8 Low-density hematite particles Average major axial 0.116 0.115 0.117 0.114 diameter (μm) Average minor axial 0.0175 0.0176 0.0177 0.0178 diameter (μm) Geometric standard 1.34 1.35 1.35 1.35 deviation σg (−) Aspect ratio (−) 6.63 6.53 6.61 6.40 S_(BET) (m²/g) 134.8 125.9 145.0 145.9 S_(TEM) (m²/g) 47.3 47.1 46.7 46.6 S_(BET)/S_(TEM) (−) 2.85 2.68 3.10 3.13 Al content (wt %) 0.67 0.68 0.67 0.67 Amount of sintering P: 1.36 P: 1.10 SiO₂: 1.65 SiO₂: 1.11 preventive (wt %) Soluble Na salt 1156 999 1678 1123 (ppm) Soluble sulfate 675 567 768 760 (ppm) pH value of 6.3 7.1 7.7 7.3 particles (−) Resin adsorptivity — — — — (%) Comp. Comp. Comp. Comp. Example Example Example Example 9 10 11 12 Low-density hematite particles Average major axial 0.116 0.197 0.195 0.190 diameter (μm) Average minor axial 0.0174 0.0288 0.0289 0.0291 diameter (μm) Geometric standard 1.36 1.33 1.33 1.32 deviation σg (−) Aspect ratio (−) 6.67 6.84 6.75 6.53 S_(BET) (m²/g) 156.9 257.5 246.2 98.8 S_(TEM) (m²/g) 47.5 28.7 28.6 28.5 S_(BET)/S_(TEM) (−) 3.30 8.98 8.61 3.47 Al content (wt %) 0.66 3.22 3.23 3.21 Amount of sintering P: 1.09 P: 2.21 SiO₂: 1.80 Al: 1.65 preventive (wt %) Soluble Na salt 1022 1324 1145 876 (ppm) Soluble sulfate 689 675 548 888 (ppm) pH value of 7.2 7.5 7.2 6.0 particles (−) Resin adsorptivity — — — — (%) Comp. Comp. Comp. Example Example Example 13 14 15 Low-density hematite particles Average major axial 0.192 0.197 0.211 diameter (μm) Average minor axial 0.0298 0.0277 0.0293 diameter (μm) Geometric standard 1.33 1.32 1.36 deviation σg (−) Aspect ratio (−) 6.44 7.11 7.20 S_(BET) (m²/g) 101.8 136.9 126.6 S_(TEM) (m²/g) 27.8 29.7 28.1 S_(BET)/S_(TEM) (−) 3.66 4.61 4.51 Al content (wt %) 3.20 3.23 0.006 Amount of sintering Ti: 1.10 P: 1.09 P: 1.63 preventive (wt %) Soluble Na salt 1361 1897 1835 (ppm) Soluble sulfate 2343 576 872 (ppm) pH value of 5.3 8.0 6.8 particles (−) Resin adsorptivity — — — (%)

TABLE 6 Example Example Example Example 18 19 20 21 Kind of low-density Example Example Example Example acicular hematite 3 4 5 6 particles Densification Temperature (° C.) 700 700 680 730 Time (min.) 30 30 60 15 High-density acicular hematite particles Average major axial 0.115 0.132 0.138 0.165 diameter (μm) Average minor axial 0.0179 0.0220 0.0223 0.0263 diameter (μm) Geometric standard 1.35 1.34 1.34 1.37 deviation σg (−) Aspect ratio (−) 6.42 6.00 6.19 6.27 S_(BET) (m²/g) 58.3 51.1 48.9 40.7 S_(TEM) (m²/g) 46.3 37.9 37.3 31.6 S_(BET)/S_(TEM) (−) 1.26 1.35 1.31 1.29 Al content (wt %) 0.67 0.67 0.67 1.25 Amount of sintering SiO₂: 0.84 P: 0.67 SiO₂: 1.38 P: 1.61 preventive (wt %) P: 1.10 Soluble Na salt 1633 2466 2018 1968 (ppm) Soluble sulfate 3378 3963 3448 3607 (ppm) pH value of 5.3 5.7 5.8 5.1 particles (−) Example Example Example Example 22 23 24 25 Kind of low-density Example Example Example Example acicular hematite 7 8 9 10 particles Densification Temperature (° C.) 650 700 690 700 Time (min.) 60 45 30 60 High-density acicular hematite particles Average major axial 0.168 0.200 0.204 0.145 diameter (μm) Average minor axial 0.0261 0.0294 0.0291 0.0244 diameter (μm) Geometric standard 1.37 1.42 1.41 1.35 deviation σg (−) Aspect ratio (−) 6.44 6.80 7.01 5.94 S_(BET) (m²/g) 45.3 41.8 42.5 51.0 S_(TEM) (m²/g) 31.8 28.1 28.3 34.2 S_(BET)/S_(TEM) (−) 1.43 1.49 1.50 1.49 Al content (wt %) 1.25 0.93 0.93 0.22 Amount of sintering Al: 3.23 P: 1.29 B: 1.78 SiO₂: 1.12 preventive (wt %) Soluble Na salt 1890 2879 3330 1356 (ppm) Soluble sulfate 3129 3330 2980 3103 (ppm) pH value of 5.3 6.1 6.2 5.2 particles (−) Example Example Example Example 26 27 28 29 Kind of low-density Example Example Example Example acicular hematite 11 12 13 14 particles Densification Temperature (° C.) 650 700 750 700 Time (min.) 60 45 15 30 High-density acicular hematite particles Average major axial 0.146 0.107 0.095 0.188 diameter (μm) Average minor axial 0.0244 0.0184 0.0193 0.0288 diameter (μm) Geometric standard 1.37 1.41 1.45 1.33 deviation σg (−) Aspect ratio (−) 5.98 5.82 4.92 6.53 S_(BET) (m²/g) 50.1 57.5 51.5 40.1 S_(TEM) (m²/g) 34.2 45.4 43.9 28.8 S_(BET)/S_(TEM) (−) 1.47 1.27 1.17 1.39 Al content (wt %) 0.22 0.51 0.52 3.22 Amount of sintering P: 1.10 P: 7.28 SiO₂: 0.85 SiO₂: 1.69 preventive (wt %) P: 1.35 Soluble Na salt 1546 1678 1329 1022 (ppm) Soluble sulfate 2980 3789 3671 3223 (ppm) pH value of 5.4 5.0 5.3 5.0 particles (−) Example Example Example 30 31 32 Kind of low-density Example Example Example acicular hematite 15 16 17 particles Densification Temperature (° C.) 700 650 680 Time (min.) 30 60 60 High-density acicular hematite particles Average major axial 0.190 0.175 0.175 diameter (μm) Average minor axial 0.0281 0.0253 0.0255 diameter (μm) Geometric standard 1.32 1.36 1.38 deviation σg (−) Aspect ratio (−) 6.76 6.52 6.86 S_(BET) (m²/g) 40.5 46.4 45.9 S_(TEM) (m²/g) 29.4 32.6 32.4 S_(BET)/S_(TEM) (−) 1.38 1.42 1.42 Al content (wt %) 3.22 4.50 4.51 Amount of sintering Ti: 3.55 P: 1.13 Al: 3.61 preventive (wt %) P: 2.44 Soluble Na salt 1129 1658 1659 (ppm) Soluble sulfate 4895 769 1345 (ppm) pH value of 4.8 7.8 7.1 particles (−)

TABLE 7 Comp. Comp. Comp. Comp. Example Example Example Example 16 17 18 19 Kind of low-density Comp. Comp. Comp. Comp. acicular hematite Example Example Example Example particles 1 2 4 5 Densification Temperature (° C.) 700 650 690 710 Time (min.) 15 15 30 60 High-density acicular hematite particles Average major axial 0.076 0.086 0.121 0.115 diameter (μm) Average minor axial 0.0321 0.0256 0.0198 0.0176 diameter (μm) Geometric standard 1.96 1.71 1.56 1.35 deviation σg (−) Aspect ratio (−) 2.37 3.36 6.11 6.53 S_(BET) (m²/g) 11.5 21.9 39.6 53.2 S_(TEM) (m²/g) 29.0 34.5 42.0 47.1 S_(BET)/S_(TEM) (−) 0.40 0.63 0.94 1.13 Al content (wt %) 0.67 0.67 0.67 0.67 Amount of sintering — — P: 1.09 P: 1.36 preventive (wt %) Soluble Na salt 1754 1845 1657 1489 (ppm) Soluble sulfate 3157 3765 3890 3678 (ppm) pH value of 5.5 5.6 5.2 5.1 particles (−) Resin adsorptivity 12.6 18.8 14.4 21.6 (%) Comp. Comp. Comp. Comp. Example Example Example Example 20 21 22 23 Kind of low-density Comp. Comp. Comp. Comp. acicular hematite Example Example Example Example particles 6 7 8 9 Densification Temperature (° C.) 560 720 730 520 Time (min.) 90 45 10 60 High-density acicular hematite particles Average major axial 0.116 0.116 0.115 0.116 diameter (μm) Average minor axial 0.0175 0.0177 0.0177 0.0174 diameter (μm) Geometric standard 1.34 1.35 1.35 1.34 deviation σg (−) Aspect ratio (−) 6.63 6.55 6.50 6.67 S_(BET) (m²/g) 61.2 53.9 58.5 73.5 S_(TEM) (m²/g) 47.3 46.8 46.8 47.5 S_(BET)/S_(TEM) (−) 1.29 1.15 1.25 1.55 Al content (wt %) 0.68 0.67 0.67 0.66 Amount of sintering P: 1.12 SiO₂: 1.63 SiO₂: 1.12 P: 1.11 preventive (wt %) Soluble Na salt 1580 1462 1765 1487 (ppm) Soluble sulfate 3217 3649 3795 3098 (ppm) pH value of 5.1 5.5 5.6 5.6 particles (−) Resin adsorptivity — — — — (%) Comp. Comp. Comp. Comp. Example Example Example Example 24 25 26 27 Kind of low-density Comp. Comp. Comp. Comp. acicular hematite Example Example Example Example particles 10 11 12 13 Densification Temperature (° C.) 650 650 600 750 Time (min.) 60 45 15 30 High-density acicular hematite particles Average major axial 0.195 0.195 0.188 0.190 diameter (μm) Average minor axial 0.0289 0.0292 0.0295 0.0300 diameter (μm) Geometric standard 1.34 1.33 1.32 1.33 deviation σg (−) Aspect ratio (−) 6.75 6.68 6.37 6.33 S_(BET) (m²/g) 41.0 43.9 51.5 40.1 S_(TEM) (m²/g) 28.6 28.3 28.1 27.7 S_(BET)/S_(TEM) (−) 1.43 1.55 1.83 1.45 Al content (wt %) 3.22 3.23 3.21 3.20 Amount of sintering P: 2.25 SiO₂: 1.83 Al: 1.63 Ti: 1.10 preventive (wt %) Soluble Na salt 2167 2156 1256 1190 (ppm) Soluble sulfate 3679 3264 3690 4678 (ppm) pH value of 6.1 6.0 5.2 4.9 particles (−) Resin adsorptivity 36.5 — — — (%) Comp. Comp. Example Example 28 29 Kind of low-density Comp. Comp. acicular hematite Example Example particles 14 15 Densification Temperature (° C.) 450 680 Time (min.) 30 30 High-density acicular hematite particles Average major axial 0.198 0.206 diameter (μm) Average minor axial 0.0278 0.0299 diameter (μm) Geometric standard 1.32 1.37 deviation σg (−) Aspect ratio (−) 7.12 6.89 S_(BET) (m²/g) 73.0 38.7 S_(TEM) (m²/g) 29.6 27.6 S_(BET)/S_(TEM) (−) 2.47 1.40 Al content (wt %) 3.23 0.006 Amount of sintering P: 1.10 P: 1.65 preventive (wt %) Soluble Na salt 2456 1280 (ppm) Soluble sulfate 3356 3103 (ppm) pH value of 5.9 5.6 particles (−) Resin adsorptivity — — (%)

TABLE 8 Example Example Example Example Example 33 34 35 36 37 Kind of Example Example Example Example Example high-density 18 19 20 21 22 acicular hematite particles Wet pulverization Yes or No Yes Yes Yes Yes Yes Amount of 0 0 0 0 0 residue on sieve (wt %) Heat treatment with aqueous alkali solution pH value (−) 13.8 13.5 13.6 13.4 13.1 Temperature 98 95 93 90 97 (° C.) Time (min.) 180 210 180 180 120 Example Example Example Example Example 38 39 40 41 42 Kind of Example Example Example Example Example high-density 23 24 25 26 27 acicular hematite particles Wet pulverization Yes or No Yes Yes Yes Yes Yes Amount of 0 0 0 0 0 residue on sieve (wt %) Heat treatment with aqueous alkali solution pH value (−) 13.8 13.7 13.4 13.7 13.5 Temperature 95 93 93 95 93 (° C.) Time (min.) 90 120 180 180 140 Example Example Example Example Example 43 44 45 46 47 Kind of Example Example Example Example Example high-density 28 29 30 31 32 acicular hematite particles Wet pulverization Yes or No Yes Yes Yes Yes Yes Amount of 0 0 0 0 0 residue on sieve (wt %) Heat treatment with aqueous alkali solution pH value (−) 13.5 13.1 13.1 13.3 13.7 Temperature 98 97 90 91 95 (° C.) Time (min.) 120 180 90 180 180

TABLE 9 Example Example Example Example 33 34 35 36 Acicular hematite particles washed with water after heat treatment with aqueous alkali solution Average major axial 0.115 0.133 0.137 0.166 diameter (μm) Average minor axial 0.0179 0.0219 0.0223 0.0262 diameter (μm) Geometric standard 1.34 1.35 1.34 1.37 deviation σg (−) Aspect ratio (−) 6.42 6.02 6.14 6.34 S_(BET) (m²/g) 57.4 52.2 49.0 41.2 S_(TEM) (m²/g) 46.3 38.0 37.3 31.7 S_(BET)/S_(TEM) (−) 1.24 1.37 1.31 1.30 Al content (wt %) 0.67 0.67 0.67 1.25 Amount of sintering SiO₂: 0.84 P: 0.38 SiO₂: 1.37 P: 0.86 preventive (wt %) P: 0.55 Soluble Na salt 111 121 98 134 (ppm) Soluble sulfate 12 15 21 11 (ppm) pH value of 9.1 9.3 8.9 9.5 particles (−) Resin adsorptivity 78.8 80.6 83.6 71.2 (%) Example Example Example Example 37 38 39 40 Acicular hematite particles washed with water after heat treatment with aqueous alkali solution Average major axial 0.168 0.199 0.202 0.144 diameter (μm) Average minor axial 0.0261 0.0293 0.0291 0.0244 diameter (μm) Geometric standard 1.37 1.41 1.41 1.35 deviation σg (−) Aspect ratio (−) 6.44 6.79 6.94 5.90 S_(BET) (m²/g) 45.5 41.9 43.1 51.9 S_(TEM) (m²/g) 31.8 28.2 28.3 34.2 S_(BET)/S_(TEM) (−) 1.43 1.49 1.52 1.52 Al content (wt %) 1.25 0.93 0.93 0.22 Amount of sintering Al: 3.23 P: 0.61 B: 0.24 SiO₂: 1.13 preventive (wt %) Soluble Na salt 142 110 108 89 (ppm) Soluble sulfate 12 21 16 9 (ppm) pH value of 9.6 9.2 9.0 8.8 particles (−) Resin adsorptivity 78.1 88.9 85.5 80.1 (%) Example Example Example Example 41 42 43 44 Acicular hematite particles washed with water after heat treatment with aqueous alkali solution Average major axial 0.145 0.106 0.095 0.188 diameter (μm) Average minor axial 0.0244 0.0183 0.0193 0.0287 diameter (μm) Geometric standard 1.37 1.41 1.45 1.33 deviation σg (−) Aspect ratio (−) 5.94 5.79 4.92 6.55 S_(BET) (m²/g) 50.5 58.0 52.3 40.3 S_(TEM) (m²/g) 34.2 45.7 43.9 28.8 S_(BET)/S_(TEM) (−) 1.48 1.27 1.19 1.40 Al content (wt %) 0.22 0.51 0.52 3.22 Amount of sintering P: 0.36 P: 2.89 SiO₂: 0.83 SiO₂: 1.68 preventive (wt %) P: 0.71 Soluble Na salt 98 124 68 96 (ppm) Soluble sulfate 16 34 46 21 (ppm) pH value of 8.8 9.3 9.0 8.9 particles (−) Resin adsorptivity 79.5 76.8 71.1 84.3 (%) Example Example Example 45 46 47 Acicular hematite particles washed with water after heat treatment with aqueous alkali solution Average major axial 0.189 0.175 0.174 diameter (μm) Average minor axial 0.0281 0.0253 0.0255 diameter (μm) Geometric standard 1.32 1.35 1.37 deviation σg (−) Aspect ratio (−) 6.73 6.92 6.82 S_(BET) (m²/g) 41.1 46.9 44.9 S_(TEM) (m²/g) 29.4 32.6 32.4 S_(BET)/S_(TEM) (−) 1.40 1.44 1.39 Al content (wt %) 3.22 4.50 4.51 Amount of sintering Ti: 3.54 P: 0.56 Al: 3.60 preventive (wt %) P: 1.13 Soluble Na salt 87 129 100 (ppm) Soluble sulfate 16 15 5 (ppm) pH value of 9.2 9.3 9.2 particles (−) Resin adsorptivity 80.8 71.9 84.6 (%)

TABLE 10 Comp. Comp. Comp. Comp. Comp. Example Example Example Example Example 30 31 32 33 34 Kind of Comp. Comp. Comp. Comp. Comp. acicular Example Example Example Example Example hematite 20 21 22 23 25 particles Wet pulverization Yes or No Yes Yes Yes No No Amount of 0 0 0 18.6 29.5 residue on sieve (wt %) Heat treatment with aqueous alkali solution pH value (−) — 12.1 13.2 13.2 10.3 Temperature — 95 68 90 97 (° C.) Time (min.) — 180 180 180 180 Comp. Comp. Comp. Comp. Example Example Example Example 35 36 37 38 Kind of acicular Comp. Comp. Comp. Comp. hematite particles Example Example Example Example 26 27 28 29 Wet pulverization Yes or No No No Yes Yes Amount of residue 30.4 21.6 0 0 on sieve (wt %) Heat treatment with aqueous alkali solution pH value (−) 13.5 13.4 9.3 13.6 Temperature 95 93 95 93 (° C.) Time (min.) 180 120 120 180

TABLE 11 Comp. Comp. Comp. Example Example Example 30 31 32 Acicular hematite particles washed with water after heat treatment with aqueous alkali solution Average major axial 0.115 0.116 0.115 diameter (μm) Average minor axial 0.175 0.0176 0.0177 diameter (μm) Geometric standard 1.34 1.35 1.34 deviation σg (−) Aspect ratio (−) 6.57 6.59 6.50 S_(BET) (m²/g) 62.0 53.8 58.4 S_(TEM) (m²/g) 47.3 47.0 46.8 S_(BET)/S_(TEM) (−) 1.31 1.14 1.25 Al content (wt %) 0.68 0.67 0.67 Amount of sintering P: 1.12 SiO₂: 1.62 SiO₂: 1.11 preventive (wt %) Soluble Na salt 712 413 378 (ppm) Soluble sulfate 436 336 168 (ppm) pH value of 6.7 7.0 8.2 particles (−) Resin adorptivity 64.1 59.3 64.6 (%) Comp. Comp. Comp. Example Example Example 33 34 35 Acicular hematite particles washed with water after heat treatment with aqueous alkali solution Average major axial 0.117 0.198 0.192 diameter (μm) Average minor axial 0.0177 0.0294 0.0297 diameter (μm) Geometric standard 1.37 1.37 1.41 deviation σg (−) Aspect ratio (−) 6.61 6.73 6.46 S_(BET) (m²/g) 73.9 43.0 51.9 S_(TEM) (m²/g) 46.7 28.1 27.9 S_(BET)/S_(TEM) (−) 1.58 1.53 1.86 Al content (wt %) 0.66 3.23 3.21 Amount of sintering P: 0.61 SiO₂: 1.80 Al: 1.65 preventive (wt %) Soluble Na salt 490 698 468 (ppm) Soluble sulfate 225 289 265 (ppm) pH value of 7.3 7.4 7.0 particles (−) Resin adorptivity 53.1 46.5 41.6 (%) Comp. Comp. Comp. Example Example Example 36 37 38 Acicular hematite particles washed with water after heat treatment with aqueous alkali solution Average major axial 0.191 0.197 0.206 diameter (μm) Average minor axial 0.0302 0.0274 0.0300 diameter (μm) Geometric standard 1.41 1.37 1.35 deviation σg (−) Aspect ratio (−) 6.32 7.19 6.87 S_(BET) (m²/g) 40.7 74.8 37.8 S_(TEM) (m²/g) 27.5 30.0 27.5 S_(BET)/S_(TEM) (−) 1.48 2.49 1.37 Al content (wt %) 3.20 3.23 0.006 Amount of sintering Ti: 1.00 P: 0.96 P: 0.61 preventive (wt %) Soluble Na salt 435 549 116 (ppm) Soluble sulfate 214 310 56 (ppm) pH value of 7.5 7.1 8.8 particles (−) Resin adorptivity 58.6 60.1 63.6 (%)

TABLE 12 Example Example Example Example 48 49 50 51 Kind of acicular Example Example Example Example hematite particles 33 34 35 36 treated with aqueous alkali solution Surface treatment Kind Sodium #3 Water Aluminum Colloidal aluminate glass sulfate silica Amount added (wt %) 5.0 1.0 1.5 3.0 Coating material Kind Al* Si* Al* Si* Amount (wt %) 4.76 0.98 1.47 2.90 Example 52 Example 53 Kind of acicular Example 37 Example 38 hematite particles treated with aqueous alkali solution Surface treatment Kind Aluminum acetate/ Aluminum sulfate/ #3 Water glass #3 Water glass Amount added (wt %) 3.0/1.0 0.5/3.0 Coating material Kind Al*/Si* Al*/Si* Amount (wt %) 2.91/0.97 0.49/2.86 Example 54 Example 55 Example 56 Kind of acicular Example Example 40 Example hematite particles 39 41 treated with aqueous alkali solution Surface treatment Kind Sodium Sodium Sodium aluminate aluminate/ aluminate Colloidal silica Amount added 10. 1.5/2.0 0.5 (wt %) Coating material Kind Al* Al*/Si* Al* Amount (wt %) 9.09 1.48/1.96 0.49 Example 57 Example 58 Example 59 Kind of acicular Example Example Example 45 hematite particles 44 43 treated with aqueous alkali solution Surface treatment Kind Aluminum #3 Water Sodium acetate glass aluminate/ Aluminum acetate Amount added 15.0 5.0 2.0/4.0 (wt %) Coating material Kind Al* Si* Al* Amount (wt %) 13.05 4.75 5.80 Example 60 Example 61 Example 62 Kind of acicular Example 45 Example Example hematite particles 46 47 treated with aqueous alkali solution Surface treatment Kind #3 Water glass/ Sodium Sodium Colloidal silica aluminate aluminate Amount added 0.2/0.3 7.5 20.0 (wt %) Coating material Kind Si* Al* Al* Amount (wt %) 0.46 6.96 16.64 Al*: aluminum hydroxide, Si*: silicon oxide

TABLE 13 Example Example Example Example 48 49 50 51 Acicular hematite particles washed with water after surface treatment Average major axial 0.115 0.133 0.137 0.165 diameter (μm) Average minor axial 0.0179 0.0220 0.0222 0.0262 diameter (μm) Geometric standard 1.35 1.35 1.34 1.36 deviation σg (−) Aspect ratio (−) 6.42 6.05 6.17 6.30 S_(BET) (m²/g) 57.2 54.0 47.8 43.6 S_(TEM) (m²/g) 46.3 37.9 37.5 31.7 S_(BET)/S_(TEM) (−) 1.23 1.43 1.28 1.38 Al content (wt %) 0.67 0.67 0.67 1.25 Amount of sintering SiO₂: 0.81 P: 0.37 SiO₂: 1.35 P: 0.81 preventive (wt %) P: 0.52 Soluble Na salt (ppm) 123 112 89 125 Soluble sulfate (ppm) 19 23 43 20 pH value of particles 9.2 9.1 9.4 9.0 (−) Resin adsorptivity (%) 80.1 81.5 80.8 88.3 Example Example Example Example 52 53 54 55 Acicular hematite particles washed with water after surface treatment Average major axial 0.167 0.200 0.201 0.144 diameter (μm) Average minor axial 0.0261 0.0293 0.0292 0.0244 diameter (μm) Geometric standard 1.37 1.42 1.41 1.35 deviation σg (−) Aspect ratio (−) 6.40 6.83 6.88 5.90 S_(BET) (m²/g) 46.6 43.9 43.9 53.8 S_(TEM) (m²/g) 31.8 28.2 28.3 34.2 S_(BET)/S_(TEM) (−) 1.47 1.56 1.55 1.57 Al content (wt %) 1.25 0.93 0.93 0.22 Amount of sintering Al: 3.19 P: 0.56 B: 0.15 SiO₂: 1.10 preventive (wt %) Soluble Na salt (ppm) 138 144 100 134 Soluble sulfate (ppm) 8 49 11 12 pH value of particles 9.5 8.9 9.3 9.3 (−) Resin adsorptivity (%) 81.9 93.6 94.2 88.9 Example Example Example Example 56 57 58 59 Acicular hematite particles washed with water after surface treatment Average major axial 0.144 0.106 0.096 0.189 diameter (μm) Average minor axial 0.0244 0.0183 0.0193 0.0288 diameter (μm) Geometric standard 1.35 1.41 1.42 1.33 deviation σg (−) Aspect ratio (−) 5.90 5.79 4.97 6.56 S_(BET) (m²/g) 50.0 56.8 54.1 38.9 S_(TEM) (m²/g) 34.2 45.7 43.9 28.7 S_(BET)/S_(TEM) (−) 1.46 1.24 1.23 1.35 Al content (wt %) 0.22 0.51 0.52 3.22 Amount of sintering P: 0.36 P: 2.66 SiO₂: 0.80 SiO₂: 1.58 preventive (wt %) P: 0.65 Soluble Na salt (ppm) 53 96 115 88 Soluble sulfate (ppm) 23 37 21 15 pH value of particles 8.8 8.9 9.0 9.1 (−) Resin adsorptivity (%) 85.6 77.6 75.6 90.6 Example 60 Example 61 Example 62 Acicular hematite particles washed with water after surface treatment Average major axial diameter 0.189 0.175 0.175 (μm) Average minor axial diameter 0.0282 0.0253 0.0254 (μm) Geometric standard deviation 1.33 1.36 1.36 σg (−) Aspect ratio (−) 6.70 6.92 6.89 S_(BET) (m²/g) 43.6 47.4 48.1 S_(TEM) (m²/g) 29.3 32.6 32.5 S_(BET)/S_(TEM) (−) 1.49 1.45 1.48 Al content (wt %) 3.22 4.50 4.51 Amount of sintering pre- Ti: 3.32 P: 0.51 Al: 3.16 vention (wt %) P: 1.10 Soluble Na salt (ppm) 129 76 102 Soluble sulfate (ppm) 13 8 23 pH value of particles (−) 9.6 9.2 9.1 Resin adsorptivity (%) 83.6 81.0 91.6

TABLE 14 Example Example Example Example Example 63 64 65 66 67 Production of non- magnetic coating film composition Kind of Example Example Example Example Example acicular 33 34 35 36 37 hematite particles Weight ratio 5.0 5.0 5.0 5.0 5.0 of particles and resin (−) Non- magnetic coating film composition Viscosity 435 410 563 384 410 (cP) Non- magnetic undercoat layer Thickness 3.4 3.4 3.5 3.5 3.4 (μm) Gloss (%) 206 200 198 198 196 Ra (nm) 6.8 7.2 7.5 7.0 8.0 Young's 121 122 124 127 129 modulus (−) (relative value) Example Example Example Example Example 68 69 70 71 72 Production of non- magnetic coating film composition Kind of Example Example Example Example Example acicular 38 39 40 41 42 hematite particles Weight ratio 5.0 5.0 5.0 5.0 5.0 of particles and resin (−) Non- magnetic coating film composition Viscosity 205 230 435 410 845 (cP) Non- magnetic undercoat layer Thickness 3.6 3.2 3.4 3.5 3.8 (μm) Gloss (%) 191 193 205 202 211 Ra (nm) 8.6 8.8 7.0 6.8 6.0 Young's 131 135 118 119 116 modulus (−) (relative value) Example Example Example Example Example 73 74 75 76 77 Production of non- magnetic coating film composition Kind of Example Example Example Example Example acicular 43 44 45 46 47 hematite particles Weight ratio 5.0 5.0 5.0 5.0 5.0 of particles and resin (−) Non- magnetic coating film composition Viscosity 896 230 230 205 205 (cP) Non- magnetic undercoat layer Thickness 3.7 3.3 3.4 3.2 3.3 (μm) Gloss (%) 214 195 197 199 195 Ra (nm) 6.3 6.8 7.0 6.8 6.7 Young's 118 128 126 122 125 modulus (−) (relative value)

TABLE 15 Example Example Example Example Example 78 79 80 81 82 Production of non- magnetic coating film composition Kind of Example Example Example Example Example acicular 48 49 50 51 52 hematite particles Weight ratio 5.0 5.0 5.0 5.0 5.0 of particles and resin (−) Non- magnetic coating film composition Viscosity 384 435 435 307 384 (cP) Non- magnetic undercoat layer Thickness 3.3 3.3 3.4 3.3 3.4 (μm) Gloss (%) 216 206 202 205 200 Ra (nm) 6.0 6.6 6.8 6.4 7.0 Young's 124 124 126 129 131 modulus (−) (relative value) Example Example Example Example Example 83 84 85 86 87 Production of non- magnetic coating film composition Kind of Example Example Example Example Example acicular 53 54 55 56 57 hematite particles Weight ratio 5.0 5.0 5.0 5.0 5.0 of particles and resin (−) Non- magnetic coating film composition Viscosity 154 128 384 333 742 (cP) Non- magnetic undercoat layer Thickness 3.5 3.5 3.4 3.3 3.5 (μm) Gloss (%) 196 196 206 206 216 Ra (nm) 7.5 7.9 6.8 6.2 5.4 Young's 135 136 121 123 120 modulus (−) (relative value) Example Example Example Example Example 88 89 90 91 92 Production of non- magnetic coating film composition Kind of Example Example Example Example Example acicular 58 59 60 61 62 hematite particles Weight ratio 5.0 5.0 5.0 5.0 5.0 of particles and resin (−) Non- magnetic coating film composition Viscosity 712 179 154 179 179 (cP) Non- magnetic undercoat layer Thickness 3.5 3.3 3.4 3.3 3.3 (μm) Gloss (%) 218 198 198 201 199 Ra (nm) 5.9 6.0 6.3 6.1 6.3 Young's 121 130 128 123 130 modulus (−) (relative value)

TABLE 16 Comp. Comp. Comp. Comp. Comp. Comp. Example Example Example Example Example Example 39 40 41 42 43 44 Production of non-magnetic coating film composition Kind of acicular hematite particles Comp. Comp. Comp. Comp. Comp. Comp. Example Example Example Example Example Example 1 16 17 3 18 19 Weight ratio of particles and resin 5.0 5.0 5.0 5.0 5.0 5.0 (−) Non-magnetic coating film composition Viscosity (cP) 12800 230 333 11776 563 435 Non-magnetic undercoat layer Thickness (μm) 3.8 3.2 3.3 4.0 3.7 3.5 Gloss (%) 56 34 78 80 148 156 Ra (nm) 84.0 116.0 56.7 46.8 31.7 28.5 Young's modulus (−) (relative 84 76 88 97 103 101 value) Comp. Comp. Comp. Comp. Comp. Comp. Example Example Example Example Example Example 45 46 47 48 49 50 Production of non-magnetic coating film composition Kind of acicular hematite particles Comp. Comp. Comp. Comp. Comp. Comp. Example Example Example Example Example Example 30 31 32 33 24 34 Weight ratio of particles and resin 5.0 5.0 5.0 5.0 5.0 5.0 (−) Non-magnetic coating film composition Viscosity (cP) 563 435 384 512 410 614 Non-magnetic undercoat layer Thickness (μm) 3.7 3.3 3.5 3.7 3.7 3.6 Gloss (%) 168 175 182 164 160 146 Ra (nm) 16.9 15.2 13.1 18.8 20.2 25.5 Young's modulus (−) (relative 106 101 107 103 109 106 value) Comp. Comp. Comp. Comp. Example Example Example Example 51 52 53 54 Production of non-magnetic coating film composition Kind of acicular hematite particles Comp. Comp. Comp. Comp. Example Example Example Example 35 36 37 38 Weight ratio of particles and resin 5.0 5.0 5.0 5.0 (−) Non-magnetic coating film composition Viscosity (cP) 666 742 410 333 Non-magnetic undercoat layer Thickness (μm) 3.8 3.4 3.5 3.2 Gloss (%) 139 148 166 198 Ra (nm) 38.6 34.5 20.4 8.0 Young's modulus (−) (relative 107 109 112 128 value)

TABLE 17 Ex. 93 Ex. 94 Ex. 95 Ex. 96 Ex. 97 Magnetic recording medium using magnetic iron-based metal particles Kind of non-magnetic Ex. 63 Ex. 64 Ex. 65 Ex. 66 Ex. 67 undercoat layer Kind of magnetic iron- (I) (I) (I) (I) (I) based metal particles Weight ratio of magnetic   5.0   5.0   5.0   5.0   5.0 particles and resin (−) Thickness of magnetic   1.1   1.2   1.2   1.1   1.1 layer (μm) Coercive force (Oe) 1940 1938 1931 1949 1930 Br/Bm (−)   0.88   0.88   0.89   0.88   0.88 Gloss (%)  239  235  233  235  230 Ra (nm)   6.4   6.8   6.9   6.4   6.9 Young's modulus (−)  133  134  136  140  140 (relative value) Durability Running durability (min)  22.6  26.7  22.3  28.9  26.4 Scratch resistance A A B A A Linear absorption   1.21   1.25   1.24   1.30   1.29 coefficient (μm⁻¹) Corrosiveness Percentage of change in   4.6   5.7   8.5   6.5   7.4 coercive force (%) Percentage of change in   6.8   7.9   7.4   6.9   5.7 Bm (%) Ex. Ex. Ex. Ex. 98 Ex. 99 100 101 102 Magnetic recording medium using magnetic iron-based metal particles Kind of non-magnetic Ex. 68 Ex. 69 Ex. 70 Ex. 71 Ex. 72 undercoat layer Kind of magnetic iron- (I) (I) (II) (II) (II) based metal particles Weight ratio of magnetic   5.0   5.0   5.0   5.0   5.0 particles and resin (−) Thickness of magnetic   1.1   1.2   1.3   1.2   1.1 layer (μm) Coercive force (Oe) 1910 1934 1710 1714 1725 Br/Bm (−)   0.89   0.88   0.87   0.87   0.88 Gloss (%)  225  221  228  229  238 Ra (nm)   7.3   7.3   6.8   6.5   5.3 Young's modulus (−)  144  146  128  131  128 (relative value) Durability Running durability (min)  30≧  30≧  22.5  24.5  18.6 Scratch resistance A A A A B Linear absorption   1.33   1.35   1.41   1.43   1.21 coefficient (μm⁻¹) Corrosiveness Percentage of change in   6.5   6.9   7.8   4.6   6.8 coercive force (%) Percentage of change in   4.8   4.9   6.8   7.2   7.8 Bm (%) Ex. Ex. Ex. Ex. Ex. 103 104 105 106 107 Magnetic recording medium using magnetic iron-based metal particles Kind of non-magnetic Ex. 73 Ex. 74 Ex. 75 Ex. 76 Ex. 77 undercoat layer Kind of magnetic iron- (II) (II) (II) (II) (II) based metal particles Weight ratio of magnetic   5.0   5.0   5.0   5.0   5.0 particles and resin (−) Thickness of magnetic   1.1   1.1   1.2   1.2   1.3 layer (μm) Coercive force (Oe) 1690 1730 1723 1698 1702 Br/Bm (−)   0.88   0.89   0.88   0.88   0.87 Gloss (%)  238  219  222  227  220 Ra (nm)   5.6   6.4   6.5   6.0   6.5 Young's modulus (−)  130  138  138  133  136 (relative value) Durability Running durability (min)  16.8  28.9  29.0  25.7  27.1 Scratch resistance B A A B A Linear absorption   1.23   1.25   1.24   1.24   1.22 coefficient (μm⁻¹) Corrosiveness Percentage of change in   7.1   8.8   3.6   4.7   4.7 coercive force (%) Percentage of change in   8.9   6.4   7.0   5.7   8.7 Bm (%) (I): Major axial diameter = 0.11 μm; Minor axial diameter = 0.018 μm; Aspect ratio = 6.1; Hc = 1880 Oe; σs = 128 emu/g; pH value = 9.9. (II): Major axial diameter = 0.14 μm; Minor axial diameter = 0.021 μm; Aspect ratio = 6.7; Hc = 1650 Oe; σs = 134 emu/g; pH value = 10.0.

TABLE 18 Ex. 108 Ex. 109 Ex. 110 Ex. 111 Ex. 112 Magnetic recording medium using magnetic iron-based metal particles Kind of non-magnetic undercoat layer Ex. 78 Ex. 79 Ex. 80 Ex. 81 Ex. 82 Kind of magnetic iron-based metal particles (I) (I) (I) (I) (I) Weight ratio of magnetic particles and resin (−)   5.0   5.0   5.0   5.0   5.0 Thickness of magnetic layer (μm)   1.1   1.1   1.2   1.1   1.1 Coercive force (Oe) 1954 1945 1940 1950 1949 Br/Bm (−)   0.89   0.88   0.89   0.89   0.89 Gloss (%)  241  238  240  237  236 Ra (nm)   6.0   6.4   6.3   6.4   6.3 Young's modulus (−) (relative value)  136  135  139  141  144 Durability Running durability (min)  28.9  29.9  27.5  30≧  28.8 Scratch resistance A A A A A Linear absorption coefficient (μm⁻¹)   1.22   1.26   1.27   1.32   1.32 Corrosiveness Percentage of change in coercive force (%)   3.2   4.6   5.3   3.8   7.1 Percentage of change in Bm (%)   4.8   6.0   5.6   5.1   4.3 Ex. 113 Ex. 114 Ex. 115 Ex. 116 Ex. 117 Magnetic recording medium using magnetic iron-based metal particles Kind of non-magnetic undercoat layer Ex. 83 Ex. 84 Ex. 85 Ex. 86 Ex. 87 Kind of magnetic iron-based metal particles (I) (I) (II) (II) (II) Weight ratio of magnetic particles and resin (−)   5.0   5.0   5.0   5.0   5.0 Thickness of magnetic layer (μm)   1.1   1.2   1.1   1.2   1.1 Coercive force (Oe) 1946 1956 1723 1734 1734 Br/Bm (−)   0.88   0.90   0.88   0.88   0.88 Gloss (%)  228  226  229  231  234 Ra (nm)   6.8   6.8   6.0   6.0   5.4 Young's modulus (−) (relative value)  146  147  133  133  132 Durability Running durability (min)  30≧  30≧  30≧  30≧  20.7 Scratch resistance A A A A A Linear absorption coefficient (μm⁻¹)   1.33   1.36   1.43   1.44   1.25 Corrosiveness Percentage of change in coercive force (%)   6.1   5.0   6.3   3.5   4.0 Percentage of change in Bm (%)   3.7   4.0   5.1   4.7   5.2 Ex. 118 Ex. 119 Ex. 120 Ex. 121 Ex. 122 Magnetic recording medium using magnetic iron-based metal particles Kind of non-magnetic undercoat layer Ex. 88 Ex. 89 Ex. 90 Ex. 91 Ex. 92 Kind of magnetic iron-based metal particles (II) (II) (II) (II) (II) Weight ratio of magnetic particles and resin (−)   5.0   5.0   5.0   5.0   5.0 Thickness of magnetic layer (μm)   1.1   1.1   1.2   1.1   1.1 Coercive force (Oe) 1708 1723 1735 1713 1732 Br/Bm (−)   0.89   0.89   0.88   0.88   0.89 Gloss (%)  237  227  230  231  225 Ra (nm)   5.4   6.1   6.3   6.4   6.2 Young's modulus (−) (relative value)  133  138  141  135  138 Durability Running durability (min)  22.8  28.7  27.8  29.5  25.8 Scratch resistance A A A A A Linear absorption coefficient (μm⁻¹)   1.24   1.25   1.24   1.23   1.25 Corrosiveness Percentage of change in coercive force (%)   3.7   6.9   2.8   4.1   3.5 Percentage of change in Bm (%)   6.1   5.8   5.9   4.3   3.6 (I): Major axial diameter = 0.11 μm; Minor axial diameter = 0.018 μm; Aspect ratio = 6.1; Hc = 1880 Oe; σs = 128 emu/g; pH value = 9.9. (II): Major axial diameter = 0.14 μm; Minor axial diameter = 0.021 μm; Aspect ratio = 6.7; Hc = 1650 Oe; σs = 134 emu/g; pH value = 10.0.

TABLE 19 Comp. Comp. Comp. Comp. Ex. 55 Ex. 56 Ex. 57 Ex. 58 Magnetic recording medium using magnetic iron-based metal particles Kind of non-magnetic undercoat Comp. Comp. Comp. Comp. layer Ex. 39 Ex. 40 Ex. 41 Ex. 42 Kind of magnetic iron-based metal (I) (I) (I) (I) particles Weight ratio of magnetic particles 5.0 5.0 5.0 5.0 and resin (−) Thickness of magnetic layer (μm) 1.3 1.2 1.2 1.2 Coercive force (Oe) 1890 1880 1895 1901 Br/Bm (−) 0.82 0.78 0.83 0.83 Gloss (%) 146 112 156 161 Ra (nm) 64.0 78.8 42.6 32.4 Young's modulus (−) (relative 93 87 99 107 value) Durability Running durability (min) 0.8 1.2 0.4 4.1 Scratch resistance D C D C Linear absorption coefficient 0.70 0.72 0.84 0.91 (μm⁻¹) Corrosiveness Percentage of change in coercive 45.6 38.9 49.0 28.6 force (%) Percentage of change in Bm (%) 25.7 25.1 36.8 24.5 Comp. Comp. Comp. Comp. Ex. 59 Ex. 60 Ex. 61 Ex. 62 Magnetic recording medium using magnetic iron-based metal particles Kind of non-magnetic undercoat Comp. Comp. Comp. Comp. layer Ex. 43 Ex. 44 Ex. 451 Ex. 46 Kind of magnetic iron-based metal (I) (I) (I) (I) particles Weight ratio of magnetic particles 5.0 5.0 5.0 5.0 and resin (−) Thickness of magnetic layer (μm) 1.2 1.3 1.1 1.3 Coercive force (Oe) 1911 1905 1918 1914 Br/Bm (−) 0.84 0.84 0.85 0.83 Gloss (%) 176 186 189 193 Ra (nm) 25.8 24.8 15.1 11.9 Young's modulus (−) (relative 113 111 117 114 value) Durability Running durability (min) 6.0 3.6 9.8 10.3 Scratch resistance C C C B Linear absorption coefficient 1.03 1.06 1.12 1.08 (μm⁻¹) Corrosiveness Percentage of change in coercive 23.6 31.3 18.0 14.7 force (%) Percentage of change in Bm (%) 28.9 23.1 18.8 14.3 Comp. Comp. Comp. Comp. Ex. 63 Ex. 64 Ex. 65 Ex. 66 Magnetic recording medium using magnetic iron-based metal particles Kind of non-magnetic undercoat Comp. Comp. Comp. Comp. layer Ex. 47 Ex. 48 Ex. 49 Ex. 50 Kind of magnetic iron-based metal (I) (I) (I) (I) particles Weight ratio of magnetic particles 5.0 5.0 5.0 5.0 and resin (−) Thickness of magnetic layer (μm) 1.1 1.2 1.1 1.0 Coercive force (Oe) 1903 1905 1896 1906 Br/Bm (−) 0.85 0.84 0.83 0.82 Gloss (%) 193 178 167 165 Ra (nm) 13.1 15.6 21.6 21.6 Young's modulus (−) (relative 121 131 123 117 value) Durability Running durability (min) 8.9 8.6 5.8 4.3 Scratch resistance C C C D Linear absorption coefficient 1.00 1.18 1.20 1.21 (μm⁻¹) Corrosiveness Percentage of change in coercive 16.8 17.9 36.9 21.7 force (%) Percentage of change in Bm (%) 15.3 17.9 23.9 18.0 Comp. Comp. Comp. Comp. Ex. 67 Ex. 68 Ex. 69 Ex. 70 Magnetic recording medium using magnetic iron-based metal particles Kind of non-magnetic undercoat Comp. Comp. Comp. Comp. layer Ex. 51 Ex. 52 Ex. 53 Ex. 54 Kind of magnetic iron-based metal (I) (I) (I) (I) particles Weight ratio of magnetic particles 5.0 5.0 5.0 5.0 and resin (−) Thickness of magnetic layer (μm) 1.3 1.3 1.2 1.1 Coercive force (Oe) 1893 1899 1913 1925 Br/Bm (−) 0.84 0.85 0.85 0.88 Gloss (%) 150 163 171 225 Ra (nm) 28.0 26.3 12.8 7.8 Young's modulus (−) (relative 123 123 124 139 value) Durability Running durability (min) 3.8 8.8 9.9 9.4 Scratch resistance D C C B Linear absorption coefficient 1.21 1.15 1.20 1.29 (μm⁻¹) Corrosiveness Percentage of change in coercive 16.8 18.6 16.0 8.6 force (%) Percentage of change in Bm (%) 21.0 16.9 13.8 6.2 (I): Major axial diameter = 0.11 μm; Minor axial diameter = 0.018 μm; Aspect ratio = 6.1; Hc = 1880 Oe; σs = 138 emu/g; pH value = 9.9.

TABLE 20 Starting Starting Starting material material material (I) (II) (III) Production of acicular goethite particles Production method (B) (C) (D) Kind of Al added Aluminum Aluminum Aluminum sulfate acetate nitrate Acicular goethite particles Average major axial diameter (μm) 0.146 0.178 0.135 Average minor axial diameter (μm) 0.0195 0.0225 0.0187 Aspect ratio (−) 7.49 7.91 7.22 Geometric standard deviation σg (−) 1.36 1.45 1.30 BET specific surface area (m²/g) 198.4 175.4 225.9 Al content (wt %) 2.31 1.23 4.56 Soluble Na salt (ppm) 415 568 1325 Soluble sulfate (ppm) 359 543 1865 pH value of particles (−) 6.8 7.2 5.2 Starting material Starting material (IV) (V) Production of acicular goethite particles Production method (A) (C) Kind of Al added Sodium aluminate Acicular goethite particles Average major axial diameter (μm) 0.201 0.264 Average minor axial diameter (μm) 0.0236 0.0318 Aspect ratio (−) 8.52 8.30 Geometric standard deviation σg 1.42 1.41 (−) BET specific surface area (m²/g) 91.8 61.2 Al content (wt %) 0.83 0.003 Soluble Na salt (ppm) 1265 514 Soluble sulfate (ppm) 387 435 pH value of particles (−) 8.6 7.1

(Note) PRODUCTION METHOD:

(A): A method of oxidizing a suspension having a pH value of not less than 11 and containing colloidal ferrous hydroxide particles which is obtained by adding not less than an equivalent of an alkali hydroxide solution to an aqueous ferrous salt solution, by passing an oxygen-containing gas thereinto at a temperature of not higher than 80° C.

(B): A method of producing spindle-shaped goethite particles by oxidizing a suspension containing FeCO₃ which is obtained by reacting an aqueous ferrous salt solution with an aqueous alkali carbonate solution, by passing an oxygen-containing gas thereinto after aging the suspension, if necessary.

(C): A method of growing acicular seed goethite particles by oxidizing a ferrous hydroxide solution containing colloidal ferrous hydroxide particles which is obtained by adding less than an equivalent of an alkali hydroxide solution or an alkali carbonate solution to an aqueous ferrous salt solution, by passing an oxygen-containing gas thereinto, thereby producing acicular seed goethite particles, adding not less than an equivalent of an alkali hydroxide solution to the Fe²⁺ in the aqueous ferrous salt solution, to the aqueous ferrous salt solution containing the acicular goethite seed particles, and passing an oxygen-containing gas into the aqueous ferrous salt solution.

(D): A method of growing acicular seed goethite particles by oxidizing a ferrous hydroxide solution containing colloidal ferrous hydroxide particles which is obtained by adding less than an equivalent of an alkali hydroxide solution or an alkali carbonate solution to an aqueous ferrous salt solution, by passing an oxygen-containing gas thereinto, thereby producing acicular seed goethite particles, and growing the obtained acicular seed goethite particles in an acidic or neutral region.

TABLE 21 Example 125 Example 126 Example 127 Kind of starting Starting material Starting Starting material in Example 123 material (I) material (I) Sintering preventive Kind Hexametaphosphate #3 Water glass #3 Water glass/ soda phosphoric acid Amount added P: 0.80 SiO₂: 1.30 SiO₂: 1.00 (wt %) P: 0.50 Heating and dehydration Temperature 320 310 350 (° C.) Time (min.)  45  60  45 Example 128 Example 129 Example 130 Kind of starting Starting material (II) Starting Starting material material (II) material ((II) Sintering preventive Kind #3 Water glass Titanyl sulfate Phosphoric acid Amount added SiO₂: 2.00 Ti: 3.00 P: 0.75 (wt %) Heating and dehydration Temperature 330 330 300 (° C.) Time (min.)  75  60  90 Example 131 Example 132 Example 133 Kind of starting Starting material Starting Starting material (III) material (IV) material (IV) Sintering preventive Kind Boric acid #3 Water glass #3 Water glass/ Hexameta- phosphate soda Amount added B: 0.50 SiO₂: 1.50 SiO₂: 0.50 (wt %) P: 0.75 Heating and dehydration Temperature 310 350 300 (° C.) Time (min.)  75  60  60

TABLE 22 Example Example Example 125 126 127 Low-density hematite particles Average major axial diameter (μm) 0.135 0.120 0.123 Average minor axial diameter (μm) 0.0191 0.0191 0.0189 Geometric standard deviation σg (−) 1.35 1.36 1.37 Aspect ratio (−) 7.07 6.28 6.51 S_(BET) (m²/g) 178.9 211.2 225.0 S_(TEM) (m²/g) 43.1 43.5 43.8 S_(BET)/S_(TEM) (−) 4.15 4.86 5.13 Al content (wt %) 0.91 2.51 2.53 Amount of sintering preventive P: 0.70 SiO₂: 1.22 SiO₂: 0.94 (wt %) P: 0.44 Soluble Na salt (ppm) 1265 1077 1356 Soluble sulfate (ppm) 569 752 865 pH value of particles (−) 6.5 7.0 7.0 Example Example Example 128 129 130 Low-density hematite particles Average major axial diameter (μm) 0.142 0.140 0.111 Average minor axial diameter (μm) 0.0201 0.0206 0.0175 Geometric standard deviation σg (−) 1.45 1.45 1.32 Aspect ratio (−) 7.06 6.80 6.34 S_(BET) (m²/g) 205.4 195.3 168.2 S_(TEM) (m²/g) 41.0 40.1 47.4 S_(BET)/S_(TEM) (−) 5.01 4.87 3.55 Al content (wt %) 1.35 1.31 4.98 Amount of sintering preventive SiO₂: 1.81 Ti: 3.22 P: 0.63 (wt %) Soluble Na salt (ppm) 1546 1759 2356 Soluble sulfate (ppm) 1056 983 2654 pH value of particles (−) 6.5 7.2 6.9 Example Example Example 131 132 133 Low-density hematite particles Average major axial diameter (μm) 0.108 0.164 0.168 Average minor axial diameter (μm) 0.0177 0.0242 0.0240 Geometric standard deviation σg (−) 1.33 1.43 1.42 Aspect ratio (−) 6.10 6.78 7.00 S_(BET) (m²/g) 175.3 138.0 146.5 S_(TEM) (m²/g) 47.0 34.1 34.3 S_(BET)/S_(TEM) (−) 3.73 4.04 4.27 Al content (wt %) 4.93 1.01 1.03 Amount of sintering preventive B: 0.21 SiO₂: 1.36 SiO₂: 0.44 (wt %) P: 0.67 Soluble Na salt (ppm) 2564 1236 1498 Soluble sulfate (ppm) 2850 854 792 pH value of particles (−) 6.5 7.7 7.9

TABLE 23 Comp. Example Comp. Example Comp. Example Comp. Example Comp. Example Comp. Example Comp. Example 71 72 73 74 75 76 77 Kind of Starting Starting Starting Starting Starting Starting Starting starting material (V) material (V) material (V) material (V) material (V) material (V) material (V) material Sintering preventive Kind — — #3 Water glass Phosphoric acid Colloidal Phosphoric acid #3 Water glass silica Amount — — SiO₂:0.75 P:1.00 SiO₂:1.25 P:0.50 SiO₂:1.50 added (wt %) Heating and dehydration Temperature 350 350 350 — 320 300 350 (° C.) Time (min.) 60 30 60 — 30 30 60 Comp. Example Comp. Example Comp. Example Comp. Example Comp. Example Comp. Example Comp. Example 78 79 80 81 82 83 84 Kind of Starting Starting Particles in Particles in Particles in Particles in Particles in starting material (V) material (V) Examples 123 Examples 123 Examples 123 Examples 123 Examples 123 material Sintering preventive Kind #3 Water glass Phosphoric acid Hexameta- #3 Water glass Boric acid Titanyl sulfate Phosphoric acid phosphate soda Amount SiO₂:1.00 P:1.00 P:1.25 SiO₂:1.50 B:0.75 Ti:0.50 P:1.00 added (wt %) Heating and dehydration Temperature 350 310 350 350 330 350 330 (° C.) Time (min.) 60 60 90 60 60 30 45

TABLE 24 Comp. Example Comp. Example Comp. Example Comp. Example Comp. Example Comp. Example Comp. Example 71 72 73 74 75 76 77 Low-density hematite particles Average major 0.213 0.214 0.214 — 0.213 0.215 0.214 axial diameter (μm) Average minor 0.0298 0.0296 0.0297 — 0.0296 0.0299 0.0298 axial diameter (μm) Geometric 1.42 1.41 1.41 — 1.42 1.43 1.41 standard deviation σg (−) Aspect ratio (−) 7.15 7.23 7.21 — 7.20 7.19 7.18 S_(BET) (m²/g) 78.9 81.5 123.8 — 131.5 125.9 135.6 S_(TEM) (m²/g) 27.6 27.8 27.7 — 27.8 27.5 27.6 S_(BET)/S_(TEM) (−) 2.86 2.93 4.47 — 4.73 4.58 4.91 Al content 0.003 0.003 0.003 — 0.003 0.003 0.003 (wt %) Amount of — — SiO₂:0.70 — SiO₂:1.38 P:0.46 SiO₂:1.26 sintering preventive (wt %) Soluble Na salt 657 756 1189 — 1245 1345 1232 (ppm) Soluble sulfate 564 567 547 — 657 589 686 (ppm) pH of particles 6.3 6.5 7.0 — 7.3 7.1 7.1 (−) Resin 8.7 — 13.8 — — — — adsorptivity (%) Comp. Example Comp. Example Comp. Example Comp. Example Comp. Example Comp. Example Comp. Example 78 79 80 81 82 83 84 Low-density hematite particles Average major 0.213 0.213 0.135 0.134 0.135 0.133 0.136 axial diameter (μm) Average minor 0.0297 0.0300 0.0191 0.0190 0.0189 0.0199 0.0201 axial diameter (μm) Geometric 1.42 1.43 1.36 1.35 1.35 1.34 1.35 standard deviation σg (−) Aspect ratio (−) 7.17 7.10 7.07 7.05 7.14 6.68 6.77 S_(BET) (m²/g) 123.6 126.5 185.9 173.6 185.0 156.9 179.2 S_(TEM) (m²/g) 27.7 27.4 43.1 43.4 43.5 41.5 41.1 S_(BET)/S_(TEM) (−) 4.46 4.61 4.31 4.00 4.25 3.78 4.36 Al content 0.003 0.003 0.91 0.91 0.91 0.91 0.91 (wt %) Amount of SiO₂:0.89 P:0.76 P:1.16 SiO₂:1.40 B:0.39 Ti:0.55 P:0.83 sintering preventive (wt %) Soluble Na salt 1426 1127 1287 1325 1124 1546 1438 (ppm) Soluble sulfate 631 568 564 678 769 867 687 (ppm) pH of particles 7.3 7.3 6.9 6.8 7.0 6.8 7.0 (−) Resin — — — — — — — adsorptivity (%)

TABLE 25 Example Example Example Example Example 134 135 136 137 138 Kind of Example Example Example Example Example low-density 125 126 127 128 129 acicular hematite particles Densification Temperature 650 680 630 730 650 (° C.) Time (min.) 20 30 60 15 90 High-density acicular hematite particles Average 0.134 0.120 0.122 0.141 0.140 major axial diameter (μm) Average 0.0192 0.0193 0.0190 0.0203 0.0206 minor axial diameter (μm) Geometric 1.38 1.41 1.41 1.48 1.47 standard deviation σg (−) Aspect ratio 6.98 6.22 6.42 6.95 6.80 (−) S_(BET) 48.9 53.8 54.1 43.6 45.3 (m²/g) S_(TEM) 42.9 43.1 43.6 40.6 40.1 (m²/g) S_(BET)/S_(TEM) 1.14 1.25 1.24 1.07 1.13 (−) Al content 0.91 2.51 2.53 1.35 1.31 (wt %) Amount of P:0.70 SiO₂:1.22 SiO₂:0.95 SiO₂:1.80 Ti:3.20 sintering P:0.44 preventive (wt %) Soluble Na 1633 2466 2018 1968 1890 salt (ppm) Soluble 2376 2879 2345 3607 2135 sulfate (ppm) pH value of 5.0 5.4 5.3 5.1 5.7 particles (−) Example Example Example Example 139 140 141 142 Kind of Example Example Example Example low-density 130 131 132 133 acicular hematite particles Densification Temperature 720 700 680 650 (° C.) Time (min.) 30 30 450 60 High-density acicular hematite particles Average 0.110 0.108 0.162 0.165 major axial diameter (μm) Average 0.0177 0.0176 0.0242 0.0242 minor axial diameter (μm) Geometric 1.36 1.37 1.46 1.46 standard deviation σg (−) Aspect ratio 6.21 6.14 6.69 6.82 (−) S_(BET) 57.5 56.5 37.4 40.0 (m²/g) S_(TEM) 47.0 47.3 34.2 34.1 (m²/g) S_(BET)/S_(TEM) 1.22 1.20 1.09 1.17 (−) Al content 4.98 4.93 1.01 1.03 (wt %) Amount of P:0.64 B:0.23 SiO₂:1.35 SiO₂:0.44 sintering P:0.68 preventive (wt %) Soluble Na 2879 3330 1356 1546 salt (ppm) Soluble 4153 4789 2176 2673 sulfate (ppm) pH value of 4.8 4.6 5.2 5.8 particles (−)

TABLE 26 Comp. Comp. Comp. Comp. Example Example Example Example 85 86 87 88 Kind of low-density Starting Comp. Comp. Comp. acicular hematite material Example Example Example particles (V) 72 74 75 Densification Temperature (° C.) 680 650 700 700 Time (min.) 30 30 30 45 High-density acicular hematite particles Average major axial 0.086 0.136 0.159 0.212 diameter (μm) Average minor axial 0.0379 0.0347 0.0330 0.0310 diameter (μm) Geometric standard 1.96 1.71 1.56 1.51 deviation σg (−) Aspect ratio (−) 2.27 3.92 4.82 6.84 S_(BET) (m²/g) 12.4 18.9 24.7 31.7 S_(TEM) (m²/g) 24.8 25.0 25.7 26.6 S_(BET)/S_(TEM) (−) 0.50 0.76 0.96 1.19 Al content (wt %) 0.003 0.003 0.003 0.003 Amount of sintering — — P: 0.87 SiO₂: 1.38 preventive (wt %) Soluble Na salt (ppm) 1578 1456 1768 1546 Soluble sulfate (ppm) 3246 3562 3125 2986 pH value of particles (−) 5.3 5.2 5.5 5.7 Resin adsorptivity (%) 7.4 10.4 11.5 18.5 Comp. Comp. Comp. Comp. Example Example Example Example 89 90 91 92 Kind of low-density Comp. Comp. Comp. Comp. acicular hematite Example Example Example Example particles 76 77 78 79 Densification Temperature (° C.) 560 720 700 570 Time (min.) 60 30 30 30 High-density acicular hematite particles Average major axial 0.214 0.211 0.212 0.213 diameter (μm) Average minor axial 0.0297 0.0299 0.0301 0.0300 diameter (μm) Geometric standard 1.42 1.43 1.46 1.42 deviation σg (−) Aspect ratio (−) 7.21 7.06 7.04 7.10 S_(BET) (m²/g) 44.0 33.5 36.5 43.2 S_(TEM) (m²/g) 27.7 27.5 27.4 27.5 S_(BET)/S_(TEM) (−) 1.59 1.22 1.33 1.57 Al content (wt %) 0.003 0.003 0.003 0.003 Amount of sintering P: 0.46 SiO₂: 1.25 SiO₂: 0.90 P: 0.76 preventive (wt %) Soluble Na salt (ppm) 1678 1539 1675 1690 Soluble sulfate (ppm) 2849 3128 2870 3176 pH value of particles (−) 5.5 5.0 5.5 5.4 Resin adsorptivity (%) — — — — Comp. Comp. Comp. Comp. Example Example Example Example 93 94 95 96 Kind of low-density Comp. Comp. Comp. Comp. acicular hematite Example Example Example Example particles 80 81 82 83 Densification Temperature (° C.) 680 680 600 750 Time (min.) 30 60 60 30 High-density acicular hematite particles Average major axial 0.133 0.134 0.135 0.130 diameter (μm) Average minor axial 0.0191 0.0192 0.0188 0.0190 diameter (μm) Geometric standard 1.36 1.36 1.35 1.35 deviation σg (−) Aspect ratio (−) 6.96 6.98 7.18 6.84 S_(BET) (m²/g) 53.1 49.6 60.7 50.0 S_(TEM) (m²/g) 43.2 42.9 43.8 43.4 S_(BET)/S_(TEM) (−) 1.23 1.16 1.39 1.15 Al content (wt %) 0.91 0.91 0.91 0.91 Amount of sintering P: 1.15 SiO₂: 1.41 B: 0.40 Ti: 0.55 preventive (wt %) Soluble Na salt (ppm) 2256 2187 1458 1297 Soluble sulfate (ppm) 2468 2678 2597 3018 pH value of particles (−) 6.2 6.0 5.5 5.7 Resin adsorptivity (%) 31.3 — — — Comp. Example 97 Kind of low-density acicular hematite particles Comp. Example 84 Densification Temperature (° C.) 450 Time (min.) 30 High-density acicular hematite particles Average major axial diameter (μm) 0.135 Average minor axial diameter (μm) 0.0189 Geometric standard deviation σg (−) 1.36 Aspect ratio (−) 7.14 S_(BET) (m²/g) 86.4 S_(TEM) (m²/g) 43.5 S_(BET)/S_(TEM) (−) 1.98 Al content (wt %) 0.91 Amount of sintering preventive (wt %) P: 0.83 Soluble Na salt (ppm) 2156 Soluble sulfate (ppm) 2658 pH value of particles (−) 5.4 Resin adsorptivity (%) —

TABLE 27 Example Example Example Example Example 143 144 145 146 147 Kind of high-density Example Example Example Example Example acicular hematite particles 134 135 136 137 138 Wet pulverization Yes or No Yes Yes Yes Yes Yes Amount of residue on sieve 0 0 0 0 0 (wt %) Heat treatment with aqueous alkali solution pH value (−) 13.7 13.6 13.5 13.8 13.9 Temperature (° C.) 98 98 95 95 97 Time (min.) 180 240 180 210 180 Example Example Example Example 148 149 150 151 Kind of high-density acicular hematite Example Example Example Example particles 139 140 141 142 Wet pulverization Yes or No Yes Yes Yes Yes Amount of residue on sieve (wt %) 0 0 0 0 Heat treatment with aqueous alkali solution pH value (−) 13.6 13.5 13.3 13.1 Temperature (° C.) 93 91 98 97 Time (min.) 150 180 240 180

TABLE 28 Example Example Example Example 143 144 145 146 Acicular hematite particles washed with water after heat treatment with aqueous alkali solution Average major axial 0.134 0.120 0.121 0.141 diameter (μm) Average minor axial 0.0192 0.0193 0.0190 0.0203 diameter (μm) Geometric standard 1.35 1.36 1.36 1.44 deviation σg (−) Aspect ratio (−) 6.98 6.22 6.37 6.95 S_(BET) (m²/g) 48.9 53.9 55.0 44.1 S_(TEM) (m²/g) 42.9 43.1 43.7 40.6 S_(BET)/S_(TEM) (−) 1.14 1.25 1.26 1.09 Al content (wt %) 0.91 2.51 2.53 1.35 Amount of sintering P: 0.35 SiO₂: 1.16 SiO₂: 0.90 SiO₂: 1.66 preventive (wt %) P: 0.21 Soluble Na salt (ppm) 89 72 68 118 Soluble sulfate (ppm) 8 6 13 21 pH value of particles (−) 9.3 9.4 9.3 9.7 Resin adsorptivity (%) 83.8 86.8 89.1 90.3 Example Example Example Example 147 148 149 150 Acicular hematite particles washed with water after heat treatment with aqueous alkali solution Average major axial 0.141 0.110 0.108 0.162 diameter (μm) Average minor axial 0.0205 0.0176 0.0176 0.0240 diameter (μm) Geometric standard 1.45 1.31 1.32 1.42 deviation σg (−) Aspect ratio (−) 6.88 6.25 6.14 6.75 S_(BET) (m²/g) 45.7 57.1 56.9 38.1 S_(TEM) (m²/g) 40.3 47.2 47.3 34.4 S_(BET)/S_(TEM) (−) 1.14 1.21 1.20 1.11 Al content (wt %) 1.31 4.98 4.93 1.01 Amount of sintering Ti: 3.22 P: 0.32 B: 0.08 SiO₂: 1.25 preventive (wt %) Soluble Na salt (ppm) 90 134 116 43 Soluble sulfate (ppm) 7 6 11 3 pH value of particles (−) 9.3 9.5 9.0 9.0 Resin adsorptivity (%) 81.4 92.1 93.8 83.9 Example 151 Acicular hematite particles washed with water after heat treatment with aqueous alkali solution Average major axial diameter (μm) 0.164 Average minor axial diameter (μm) 0.0240 Geometric standard deviation σg (−) 1.42 Aspect ratio (−) 6.83 S_(BET) (m²/g) 39.7 S_(TEM) (m²/g) 34.4 S_(BET)/S_(TEM) (−) 1.15 Al content (wt %) 1.03 Amount of sintering preventive (wt %) SiO₂: 0.43 P: 0.30 Soluble Na salt (ppm) 25 Soluble sulfate (ppm) 4 pH value of particles (−) 8.9 Resin adsorptivity (%) 86.9

TABLE 29 Comp. Comp. Comp. Comp. Example Example Example Example 98 99 100 101 Kind of acicular hematite Comp. Comp. Comp. Comp. particles Example Example Example Example 89 90 91 92 Wet pulverization Yes or No Yes Yes Yes No Amount of residue on 0 0 0 21.8 sieve (wt %) Heat treatment with aqueous alkali solution pH value (−) — 12.0 13.1 13.1 Temperature (° C.) — 95 58 90 Time (min.) — 180 180 180 Comp. Comp. Comp. Comp. Example Example Example Example 102 103 104 105 Kind of acicular hematite Comp. Comp. Comp. Comp. particles Example Example Example Example 94 95 96 97 Wet pulverization Yes or No No No Yes Yes Amount of residue on 31.8 29.7 0 0 sieve (wt %) Heat treatment with aqueous alkali solution pH value (−) 10.5 13.3 13.3 9.1 Temperature (° C.) 90 90 40 95 Time (min.) 180 180 180 180

TABLE 30 Comp. Comp. Comp. Comp. Example Example Example Example 98 99 100 101 Acicular hematite particles washed with water after heat treatment with aqueous alkali solution Average major axial 0.214 0.211 0.212 0.213 diameter (μm) Average minor axial 0.0297 0.0298 0.0300 0.0300 diameter (μm) Geometric standard 1.41 1.42 1.43 1.42 deviation σg (−) Aspect ratio (−) 7.21 7.08 7.07 7.10 S_(BET) (m²/g) 43.8 33.9 36.8 43.2 S_(TEM) (m²/g) 27.7 27.6 27.5 27.4 S_(BET)/S_(TEM) (−) 1.58 1.23 1.34 1.57 Al content (wt %) 0.004 0.004 0.004 0.004 Amount of sintering P: 0.46 SiO₂: 1.24 SiO₂: 0.88 P: 0.40 preventive (wt %) Soluble Na salt (ppm) 785 456 371 326 Soluble sulfate (ppm) 489 325 173 168 pH value of particles (−) 6.7 6.6 7.3 7.1 Resin adsorptivity (%) 35.7 44.6 50.7 37.5 Comp. Comp. Comp. Comp. Example Example Example Example 102 103 104 105 Acicular hematite particles washed with water after heat treatment with aqueous alkali solution Average major axial 0.134 0.135 0.131 0.135 diameter (μm) Average minor axial 0.0192 0.0188 0.0190 0.0189 diameter (μm) Geometric standard 1.37 1.36 1.35 1.36 deviation σg (−) Aspect ratio (−) 6.98 7.18 6.89 7.14 S_(BET) (m²/g) 50.0 61.1 50.3 88.1 S_(TEM) (m²/g) 42.9 43.8 43.4 43.5 S_(BET)/S_(TEM) (−) 1.16 1.40 1.16 2.02 Al content (wt %) 0.91 0.91 0.91 0.91 Amount of sintering SiO₂: 1.41 B: 0.18 Ti: 0.56 P: 0.84 preventive (wt %) Soluble Na salt (ppm) 467 345 356 487 Soluble sulfate (ppm) 256 177 170 290 pH value of particles (−) 7.0 7.4 7.3 6.8 Resin adsorptivity (%) 46.8 53.7 53.1 45.9

TABLE 31 Example Example Example Example 152 153 154 155 Kind of acicular Example Example Example Example hematite particles 143 144 145 146 treated with aqueous alkali solution Surface treatment Kind Sodium #3 Water Sodium Colloidal aluminate glass aluminate silica Amount added (wt %) 3.0  1.5  1.5  3.0  Coating material Kind Al* Si* Al* Si* Amount (wt %) 2.91 1.45 1.47 2.89 Example 156 Example 157 Kind of acicular Example 147 Example 148 hematite particles treated with aqueous alkali solution Surface treatment Kind Aluminum acetate/ Sodium #3 Water glass aluminate/ Colloidal silica Amount added (wt %) 5.0/1.0 1.0/5.0 Coating material Kind Al*/Si* Al*/Si* Amount (wt %) 4.73/0.96 0.98/4.66 Example Example Example 158 159 160 Kind of acicular Example Example 150 Example hematite particles 149 151 treated with aqueous alkali solution Surface treatment Kind Sodium Aluminum acetate/ Sodium aluminate Colloidal silica aluminate Amount added (wt %) 10.0  1.5/2.0 0.5  Coating material Kind Al* Al*/Si* Al* Amount (wt %) 8.99 1.47/1.93 0.49 Al*: aluminum hydroxide, Si*: silicon oxide

TABLE 2 Example Example Example Example 152 153 154 155 Acicular hematite particles washed with water after surface treatment Average major axial 0.134 0.121 0.121 0.141 diameter (μm) Average minor axial 0.0192 0.0193 0.0190 0.0202 diameter (μm) Geometric standard 1.35 1.36 1.36 1.44 deviation σg (−) Aspect ratio (−) 6.98 6.27 6.37 6.98 S_(BET) (m²/g) 49.3 54.1 56.1 46.9 S_(TEM) (m²/g) 42.9 43.0 43.7 40.8 S_(BET)/S_(TEM) (−) 1.15 1.26 1.28 1.15 Al content (wt %) 0.91 2.51 2.53 1.35 Amount of sintering P: 0.33 SiO₂: 1.16 SiO₂: 0.90 SiO₂: 1.66 preventive (wt %) P: 0.20 Soluble Na salt 56 63 78 96 (ppm) Soluble sulfate 3 3 5 12 (ppm) pH value of 9.2 9.4 9.3 9.1 particles (−) Resin adsorptivity 85.1 87.0 90.1 92.5 (%) Example Example Example Example 156 157 158 159 Acicular hematite particles washed with water after surface treatment Average major axial 0.140 0.109 0.108 0.162 diameter (μm) Average minor axial 0.0204 0.0176 0.077 0.0239 diameter (μm) Geometric standard 1.44 1.31 1.31 1.42 deviation σg (−) Aspect ratio (−) 6.86 6.19 6.10 6.78 S_(BET) (m²/g) 46.0 58.3 59.7 39.5 S_(TEM) (m²/g) 40.5 47.2 47.0 34.6 S_(BET)/S_(TEM) (−) 1.14 1.23 1.27 1.14 Al content (wt %) 1.31 4.98 4.93 1.01 Amount of sintering Ti: 3.04 P: 0.30 B: 0.07 SiO₂: 1.25 preventive (wt %) Soluble Na salt 54 91 89 32 (ppm) Soluble sulfate 4 5 2 8 (ppm) pH value of 9.3 9.5 9.5 9.3 particles (−) Resin adsorptivity 86.9 92.0 94.6 89.0 (%) Example 160 Acicular hematite particles washed with water after surface treatment Average major axial 0.163 diameter (μm) Average minor axial 0.0240 diameter (μm) Geometric standard 1.41 deviation σg (−) Aspect ratio (−) 6.79 S_(BET) (m²/g) 40.1 S_(TEM) (m²/g) 34.4 S_(BET)/S_(TEM) (−) 1.17 Al content (wt %) 1.03 Amount of sintering SiO₂: 0.43 preventive (wt %) P: 0.30 Soluble Na salt 27 (ppm) Soluble sulfate 4 (ppm) pH value of 9.1 particles (−) Resin adsorptivity 90.4 (%)

TABLE 33 Example Example Example Example Example 161 162 163 164 165 Production of non-magnetic coating film composition Kind of acicular Example Example Example Example Example hematite 143 144 145 146 147 particles Weight ratio of 5.0 5.0 5.0 5.0 5.0 particles and resin (−) Non-magnetic coating film composition Viscosity (cP) 384 435 410 307 333 Non-magnetic undercoat layer Thickness (μm) 3.4 3.3 3.4 3.4 3.2 Gloss (%) 207 211 215 207 209 Ra (nm) 6.4 6.0 6.0 6.4 6.6 Young's modulus 128 124 125 129 131 (−) (relative value) Example Example Example Example Example 166 167 168 169 170 Production of non-magnetic coating film composition Kind of acicular Example Example Example Example Example hematite 148 149 150 151 152 particles Weight ratio of 5.0 5.0 5.0 5.0 5.0 particles and resin (−) Non-magnetic coating film composition Viscosity (cP) 512 563 256 256 282 Non-magnetic undercoat layer Thickness (μm) 3.5 3.3 3.3 3.4 3.3 Gloss (%) 218 216 202 205 212 Ra (nm) 5.8 5.7 6.1 6.2 5.9 Young's modulus 122 121 131 132 129 (−) (relative value) Example Example Example Example Example 171 172 173 174 175 Production of non-magnetic coating film composition Kind of acicular Example Example Example Example Example hematite 153 154 155 156 157 particles Weight ratio of 5.0 5.0 5.0 5.0 5.0 particles and resin (−) Non-magnetic coating film composition Viscosity (cP) 333 307 205 230 486 Non-magnetic undercoat layer Thickness (μm) 3.2 3.3 3.2 3.2 3.4 Gloss (%) 218 223 217 218 225 Ra (nm) 5.6 5.7 6.0 6.2 5.5 Young's modulus 125 125 130 131 125 (−) (relative value) Example Example Example 176 177 178 Production of non-magnetic coating film composition Kind of acicular Example Example Example hematite 158 159 160 particles Weight ratio of 5.0 5.0 5.0 particles and resin (−) Non-magnetic coating film composition Viscosity (cP) 435 230 205 Non-magnetic undercoat layer Thickness (μm) 3.3 3.3 3.4 Gloss (%) 227 209 210 Ra (nm) 5.4 6.0 5.8 Young's modulus 124 133 133 (−) (relative value)

TABLE 34 Comp. Comp. Comp. Comp. Comp. Example Example Example Example Example 106 107 108 109 110 Production of non-magnetic coating film composition Kind of acicular Starting Comp. Comp. Comp. Comp. hematite material Example Example Example Example particles (V) 85 86 73 87 Weight ratio of 5.0 5.0 5.0 5.0 5.0 particles and resin (−) Non-magnetic coating film composition Viscosity (cP) 10240 128 154 14080 207 Non-magnetic undercoat layer Thickness (μm) 3.7 3.2 3.3 3.6 3.3 Gloss (%) 35 42 68 73 135 Ra (nm) 118.0 95.4 65.2 47.2 37.8 Young's modulus 96 98 103 100 113 (−) (relative value) Comp. Comp. Comp. Comp. Comp. Example Example Example Example Example 111 112 113 114 115 Production of non-magnetic coating film composition Kind of acicular Comp. Comp. Comp. Comp. Comp. hematite Example Example Example Example Example particles 88 98 99 100 101 Weight ratio of 5.0 5.0 5.0 5.0 5.0 particles and resin (−) Non-magnetic coating film composition Viscosity (cP) 384 973 333 384 435 Non-magnetic undercoat layer Thickness (μm) 3.4 3.3 3.2 3.3 3.3 Gloss (%) 146 172 175 171 154 Ra (nm) 29.0 17.0 13.0 14.2 32.6 Young's modulus 110 115 119 113 108 (−) (relative value) Comp. Comp. Comp. Comp. Comp. Example Example Example Example Example 116 117 118 119 120 Production of non-magnetic coating film composition Kind of acicular Comp. Comp. Comp. Comp. Comp. hematite Example Example Example Example Example particles 93 102 103 104 105 Weight ratio of 5.0 5.0 5.0 5.0 5.0 particles and resin (−) Non-magnetic coating film composition Viscosity (cP) 512 410 768 384 1229 Non-magnetic undercoat layer Thickness (μm) 3.4 3.3 3.4 3.3 3.5 Gloss (%) 164 185 188 194 191 Ra (nm) 19.6 10.8 10.2 9.2 9.6 Young's modulus 96 116 113 118 108 (−) (relative value)

TABLE 35 magnetic magnetic magnetic magnetic iron-based iron-based iron-based iron-based alloy alloy alloy alloy Kind of magnetic particles particles particles particles particles (a) (b) (c) (d) Average major 0.110 0.098 0.101 0.125 axial diameter (μm) Average minor 0.0150 0.0134 0.0144 0.0184 axial diameter (μm) Aspect ratio (−) 7.33 7.31 7.01 6.79 Geometric 1.36 1.35 1.38 1.35 standard deviation (−) Coercive force 1915 1938 2065 1896 (Oe) Saturation 131.6 130.5 128.9 130.8 magnetization (emu/g) Content of existent Al Central portion 2.61 1.32 1.38 0.01 (wt %) Surface layer 1.36 2.84 2.65 0.01 portion (wt %) Surface coating 0.01 0.01 0.78 0.01 film (wt %) Content of 0.01 0.36 2.78 0.01 existent Nd (wt %) Resin 72.5 80.1 83.6 57.6 adsorptivity (%)

TABLE 36 Ex. Ex. Ex. Ex. Ex. Ex. Ex. Ex. Ex. Ex. Ex. Ex. Ex. Ex. Ex. Ex. Ex. Ex. 179 180 181 182 183 184 185 186 187 188 189 190 191 192 193 194 195 196 Magnetic recording medium using magnetic iron-based metal particles Kind of non- Ex. Ex. Ex. Ex. Ex. Ex. Ex. Ex. Ex. Ex. Ex. Ex. Ex. Ex. Ex. Ex. Ex. Ex. magnetic undercoat 161 162 163 164 165 166 167 168 169 170 171 172 173 174 175 176 177 178 layer Kind of magnetic * (a) (a) (a) (a) * * (b) (b) (a) (b) (b) (c) (c) (c) (c) (c) (c) iron-based metal particles Weight ratio of 5.0 5.0 5.0 5.0 5.0 5.0 5.0 5.0 5.0 5.0 5.0 5.0 5.0 5.0 5.0 5.0 5.0 5.0 magnetic particles and resin (−) Thickness of 1.0 1.1 1.1 1.2 1.1 1.1 1.1 1.1 1.0 1.0 1.0 1.1 1.1 1.1 1.1 1.1 1.0 1.0 magnetic layer (μm) Coercive force (Oe) 1978 1990 1985 1978 1983 1967 1971 1998 1989 1965 1987 1985 2135 2148 2153 2121 2118 2147 Br/Bm (−) 0.88 0.88 0.88 0.88 0.89 0.88 0.88 0.89 0.89 0.88 0.88 0.89 0.89 0.89 0.90 0.91 0.90 0.89 Gloss (%) 232 236 236 228 230 231 235 219 223 238 240 242 235 232 245 241 228 226 Ra (nm) 6.2 6.0 6.0 6.4 6.4 6.2 6.0 5.8 6.0 5.8 5.4 5.2 5.9 5.9 5.5 5.9 6.0 6.2 Young's modulus 132 128 130 133 134 127 125 134 133 134 130 128 134 135 129 127 139 138 (−) (relative value) Durability Running durability 30≦ 29.6 25.8 28.4 26.5 30≦ 30≦ 30≦ 30≦ 29.4 30≦ 30≦ 30≦ 30≦ 30≦ 30≦ 30≦ 30≦ (min) Scratch resistance A A B A B A A A A A A A A A A A A A Linear absorption 1.23 1.24 1.25 1.28 1.30 1.22 1.23 1.31 1.33 1.24 1.25 1.24 1.28 1.30 1.23 1.22 1.34 1.33 coefficient (μm⁻¹) Corrosiveness Percentage of 3.6 4.6 5.3 5.1 6.2 4.8 4.9 3.7 2.1 6.4 4.1 5.3 2.6 1.8 2.5 2.7 1.6 2.7 change in coercive force (%) Percentage of 4.8 6.9 5.8 5.9 7.5 5.1 3.9 5.5 4.1 5.6 5.7 4.3 4.0 3.2 2.7 2.5 1.8 1.4 change in Bm (%) (Note) *: Particles in Example 124 (a): magnetic iron-based metal particles (a) (b): magnetic iron based metal particles (b) (c): magnetic iron-based metal particles (c)

TABLE 37 Co- Co- Co- Co- Co- Co- Co- Co- Co- Co- Co- Co- Co- Co- Co- mp. mp. mp. mp. mp. mp. mp. mp. mp. mp. mp. mp. mp. mp. mp. Ex. Ex. Ex. Ex. Ex. Ex. Ex. Ex. Ex. Ex. Ex. Ex. Ex. Ex. Ex. 121 122 123 124 125 126 127 128 129 130 131 132 133 134 135 Magnetic recording medium using magnetic iron-based metal particles Kind of non- Co- Co- Co- Co- Co- Co- Co- Co- Co- Co- Co- Co- Co- Co- Co- magnetic undercoat mp. mp. mp. mp. mp. mp. mp. mp. mp. mp. mp. mp. mp. mp. mp. layer Ex. Ex. Ex. Ex. Ex. Ex. Ex. Ex. Ex. Ex. Ex. Ex. Ex. Ex. Ex. 106 107 108 109 110 111 112 113 114 115 116 117 118 119 120 King of magnetic * (a) (a) (a) (a) (a) (a) (a) (a) (a) (d) (d) (d) (d) (d) iron-based metal particles Weight ratio of 5.0 5.0 5.0 5.0 5.0 5.0 5.0 5.0 5.0 5.0 5.0 5.0 5.0 5.0 5.0 magnetic particles and resin (−) Thickness of 1.3 1.2 1.2 1.2 1.2 1.3 1.1 1.3 1.1 1.2 1.1 1.0 1.3 1.3 1.2 magnetic layer (μm) Coercive force (Oe) 1910 1923 1934 1932 1940 1947 1934 1965 1972 1943 1896 1906 1893 1899 1913 Br/Bm (−) 0.79 0.78 0.79 0.80 0.83 0.84 0.85 0.85 0.85 0.83 0.85 0.85 0.86 0.86 0.85 Gloss (%) 134 142 164 168 177 179 193 197 192 169 180 196 206 213 215 Ra (nm) 73.0 69.7 41.6 38.9 26.4 25.0 16.3 11.2 12.0 28.6 21.7 10.8 9.6 8.8 8.2 Young's modulus 102 102 108 115 119 113 119 124 116 113 99 121 119 123 116 (−) (relative value) Durability Running durability 0.6 0.6 0.8 3.7 6.0 4.6 10.2 13.5 9.0 9.3 13.5 16.5 18.3 19.6 17.4 (min) Scratch resistance D D D D D D C C D C C C C C C Linear absorption 0.82 0.97 1.02 1.04 1.06 1.08 1.17 1.18 1.16 1.15 1.11 1.21 1.23 1.23 1.24 coefficient (μm⁻¹) Corrosiveness Percentage of 47.5 36.7 38.0 32.6 23.1 34.2 20.1 14.6 17.4 18.8 37.9 21.8 18.6 14.8 18.0 change in coercive force (%) Percentage of 35.8 45.1 38.5 34.6 31.4 26.8 28.2 18.7 18.7 21.5 32.8 28.0 27.9 21.8 16.9 change in Bm (%) (Note) *: Particles in Example 124 (a): magnetic iron-based metal particles (a) (d): magnetic iron based metal particles (d) 

What is claimed is:
 1. A magnetic recording medium comprising: a non-magnetic substrate; a non-magnetic undercoat layer comprising a coating film composition comprising non-magnetic acicular hematite particles and a binder resin, which is formed on said non-magnetic substrate; and a magnetic recording layer comprising a coating film composition comprising magnetic particles containing iron as a main ingredient and a binder resin, which is formed on said non-magnetic undercoat layer, wherein said non-magnetic acicular hematite particles contain 0.05 to 50 wt % of aluminum, calculated as Al, approximately uniformly within the particles, have an average major axial diameter of not more than 0.3 μm, a pH value of said particles of not less than 8, and contain soluble sodium salts of not more than 300 ppm soluble sodium, calculated as Na, and soluble sulfates of not more than 150 ppm soluble sulfate, calculated as SO₄; and wherein said magnetic particles containing iron as a main ingredient comprising iron and aluminum of 0.05 to 10% by weight, calculated as Al.
 2. A magnetic recording medium according to claim 1, wherein said acicular hematite particles are acicular hematite particles containing aluminum of 0.05 to 50% by weight, calculated as Al, having an average major axial diameter of not more than 0.3 μm, an average minor axial diameter of 0.0025 to 0.15 μm, an aspect ratio of not less than 2:1, a BET specific surface area (S_(BET)) of not less than 35 m²/g, a geometrical standard deviation of not more than 1.50, a resin adsorptivity of not less than 65%, and an S_(BET)/S_(TEM) value of 0.5 to 2.5, wherein said S_(TEM) is a value calculated from the major axial diameter and the minor axial diameter of said particles which were measured from said particles in an electron micrograph, and a pH value of the particles of not less than 8, containing soluble sodium salts of not more than 300 ppm soluble sodium, calculated as Na, and soluble sulfates of not more than 150 ppm soluble sulfate, calculated as SO₄.
 3. A magnetic recording medium according to claim 1, wherein said magnetic particles containing iron as a main ingredient comprise 50 to 99% by weight of iron, 0.05 to 10% by weight of aluminum, and at least one element selected from the group consisting of Co, Ni, P, Si, Zn, Ti, Cu, B, Nd, La and Y.
 4. A magnetic recording medium according to claim 1, wherein said magnetic particles containing iron as a main ingredient comprise 50 to 99% by weight of iron, 0.05 to 10% by weight of aluminum, and at least one rare earth metal selected from the group consisting of Nd, La and Y.
 5. A magnetic recording medium according to claim 1, wherein said magnetic particles containing iron as a main ingredient have an average major axial diameter of 0.01 to 0.50 μm, an average minor axial diameter of 0.0007 to 0.17 μm, an aspect ratio of not less than 3:1, a resin adsorptivity of not less than 65%, a coercive force of 1200 to 3200 Oe, and a saturation magnetization of 100 to 170 emu/g.
 6. A magnetic recording medium according to claim 1, which further have an coercive force of 900 to 3500 Oe, a squareness of 0.85 to 0.95, a gloss of 190 to 300%, a surface roughness of not more than 12.0 nm, a linear adsorption coefficient of 1.10 to 2.00 μm⁻¹, a percentage of change in said coercive force of not more than 10.0%, and a percentage of change in said saturation magnetization flux of not more than 10.0%.
 7. A magnetic recording medium according to claim 1, wherein said acicular hematite particles are acicular hematite particles containing aluminum of 0.5 to 50% by weight, calculated as Al, having an average major axial diameter of 0.005 to 0.3 μm and a pH value of the particles of 8.5 to 12, and containing soluble sodium salts of 0.01 to 250 ppm soluble sodium, calculated as Na, and soluble sulfates of 0.01 to 70 ppm soluble sulfate, calculated as SO₄.
 8. A magnetic recording medium according to claim 1, wherein said acicular hematite particles are acicular hematite particles containing aluminum of 0.05 to 50% by weight, calculated as Al, having an average major axial diameter of not more than 0.3 μm, an average minor axial diameter of 0.01 to 0.10 μm, an aspect ratio of 3:1 to 20:1, a BET specific surface area of 40 to 150 m²/g, a geometrical standard deviation of 1.01 to 1.40, a resin adsorptivity of not less than 70%, and an S_(BET)/S_(TEM) value of 0.7 to 2.0, and a pH value of the particles of not less than 8, and containing soluble sodium salts of not more than 300 ppm soluble sodium, calculated as Na, and soluble sulfates of not more than 150 ppm soluble sulfate, calculated as SO₄.
 9. A magnetic recording medium according to claim 1, wherein said acicular hematite particles are acicular hematite particles containing aluminum of 0.05 to 50% by weight, calculated as Al, having an average major axial diameter of not more than 0.3 μm and a pH value of the particles of not less than 8, containing soluble sodium salts of not more than 300 ppm soluble sodium, calculated as Na, and soluble sulfates of not more than 150 ppm soluble sulfate, calculated as SO₄, and having a coating comprising at least one member selected from the group consisting of a hydroxide of aluminum, an oxide of aluminum, a hydroxide of silicon and an oxide of silicon, which is coated on the surfaces of said acicular hematite particles.
 10. A magnetic recording medium according to claim 1, wherein said acicular hematite particles are acicular hematite particles containing aluminum of 0.05 to 50% by weight, calculated as Al, having an average major axial diameter of not more than 0.3 μm and a pH value of the particles of not less than 8, containing soluble sodium salts of not more than 300 ppm soluble sodium, calculated as Na, and soluble sulfates of not more than 150 ppm soluble sulfate, calculated as SO₄, and having a coating comprising at least one member selected from the group consisting of a hydroxide of aluminum, an oxide of aluminum, a hydroxide of silicon and an oxide of silicon, which is coated on the surfaces of said acicular hematite particles in an amount of coating material of 0.01 to 50 wt % calculated as either of Al and SiO₂ based on the total weight of particles.
 11. A magnetic recording medium comprising: a non-magnetic substrate; a non-magnetic undercoat layer comprising a coating film composition comprising non-magnetic acicular hematite particles containing aluminum of 0.05 to 50% by weight, calculated as Al, approximately uniformly within the particles, having an average major axial diameter of not more than 0.3 μm and a pH value of the particles of not less than 8, and containing soluble sodium salts of not more than 300 ppm soluble sodium, calculated as Na, and soluble sulfates of not more than 150 ppm soluble sulfate, calculated as SO₄ and a binder resin, which is formed on said non-magnetic substrate; and a magnetic recording layer comprising a coating film composition comprising magnetic particles containing iron as a main ingredient and a binder resin, which is formed on said non-magnetic undercoat layer.
 12. A magnetic recording medium comprising: a non-magnetic substrate; a non-magnetic undercoat layer comprising a coating film composition comprising non-magnetic acicular hematite particles containing 0.05 to 50% by weight of aluminum, calculated as Al, approximately uniformly within the particles, having an average major axial diameter of not more than 0.3 μm and a pH value of the particles of not less than 8, and containing soluble sodium salts of not more than 300 ppm soluble sodium, calculated as Na, and soluble sulfates of not more than 150 ppm soluble sulfate, calculated as SO₄ and a binder resin, which is formed on said non-magnetic substrate; and a magnetic recording layer comprising a coating film composition comprising magnetic particles containing iron as a main ingredient and a binder resin, which is formed on said non-magnetic undercoat layer.
 13. A magnetic recording medium according to claim 11 or 12, wherein said magnetic particles containing iron as a main ingredient comprising 50 to 99 wt % of iron, and at least one element selected from the group consisting of Co, Al, Ni, P, Si, Zn, Ti, Cu, B, Nd, La and Y.
 14. A magnetic recording medium according to claim 11 or 12, which further have a coercive force of 900 to 3500 Oe, a squareness of 0.85 to 0.95, a gloss of 190 to 300%, a surface roughness of not more than 12.0 nm, a linear adsorption coefficient of 1.10 to 2.00 μm⁻¹, a percentage of change in said coercive force of not more than 10.0%, and a percentage of change in said saturation magnetization flux of not more than 10.0%. 